Coverage Guideline

This document addresses cryosurgical techniques for peripheral nerves that create a temporary nerve block through application of extreme cold to the selected site for treatment. These techniques are known as cryoneurolysis, cryoanalgesia, and cryoablation of peripheral nerves.

Note: Please see the following related documents for additional information:

• CG-SURG-89 Radiofrequency Neurolysis and Pulsed Radiofrequency Therapy for Trigeminal Neuralgia
• SURG.00100 Cryoablation for Plantar Fasciitis and Plantar Fibroma
• SURG.00140 Peripheral Nerve Blocks for Treatment of Neuropathic Pain
• SURG.00142 Genicular Procedures for Treatment of Knee Pain
• SURG.00144 Occipital and Sphenopalatine Ganglion Nerve Block Therapy for the Treatment of Headache and Neuralgia

Investigational and Not Medically Necessary:

Cryosurgical techniques (for example, cryoneurolysis and cryoablation) of peripheral nerves are considered investigational and not medically necessary for all indications.

Peripheral Nerve Pain

Cryoneurolysis has been proposed as a treatment for peripheral nerve pain; however, there have been a limited number of studies published in the peer-reviewed literature addressing the use of this surgical procedure.

In 2016, Dasa and colleagues published a retrospective review of 100 individuals who underwent total knee arthroplasty (TKA) to compare perioperative pain management with and without cryoneurolysis. Cryoneurolysis was performed on the treatment group (n=50) 5 days prior to each TKA as part of a perioperative multimodal pain management program. The control group (n=50) did not receive cryoneurolysis. The results showed a significantly lower number of individuals in the treatment group with a length of stay (LOS) of greater than or equal to 2 days when compared to the control group (6% versus 67%, p<0.0001); however, no significant difference between groups was noted for 0 days and 1 day LOS. “The mean ± SE cumulative morphine use during the 12 weeks following surgery was significantly lower for the treatment versus control group (2069.12 ± 132.09 mg vs. 3764.42 ± 287.95 mg, p<0.0001)” (Dasa, 2016). Other evaluated outcomes included mean scores on the Knee Injury and Osteoarthritis Outcome Score (KOOS), Western Ontario and McMaster Universities Arthritis Index (WOMAC), Oxford Knee Score, 12-item Short Form Health Survey (SF-12), and Patient-reported Outcomes Measurement Information System (PROMIS). Significant reductions in the KOOS from baseline to the 6- and 12-week post-operative visits were noted in the treatment group when compared to the control group (p=0.0037 at 6 weeks; p=0.0011 at 12 weeks), in the PROMIS pain intensity scores from baseline to 2 weeks post-surgery (p<0.0001), and also in the PROMIS pain interference scores from baseline to 6 weeks post-surgery (p<0.0001); however, the absolute values of the differences were not reported and there was overlap in the supplemental data. No significant results were noted in other outcomes. No complications were reported due to cryoneurolysis and the most common side effect was local bruising. There were several limitations to this study, including the retrospective, nonrandomized design, and lack of blinding. With the study being single-center and single-surgeon, there is limited generalizability of the results. Furthermore, no disclosure or denial of conflict of interest was reported.

Yoon and colleagues (2016) reported on a prospective study evaluating cryoneurolysis as a treatment for refractory peripheral neuropathic pain. The study was approved for 144 individuals; however, only 28 individuals were screened and 22 were included in the study. All participants were treated with cryoneurolysis for peripheral neuropathy after failure of first- and second-line therapy. Results showed a significant decrease in self-reported pain using a visual analog scale (VAS) at 1 month (p=0.0001), 3 months (p=0.0002), 6 months (p=0.002), and 12 months (p=0.03) posttreatment. Cryoneurolysis had to be repeated for 11 (50%) individuals within 12 months of the original treatment. No complications were reported. While this study resulted in positive outcomes, the small sample size and lack of comparator group limits the applicability of the data. In addition, the authors did not disclose the reason for the large gap between the number of individuals approved for the study and the number of individuals screened for the study, which raises concerns for selection bias.

In 2017, Radnovich and colleagues published the results of a multicenter, randomized, double-blind, sham-controlled trial that evaluated cryoneurolysis for the treatment of pain and symptoms of knee osteoarthritis. From April 2013 to June 2016, 180 individuals were recruited and enrolled into either the active treatment group (n=121) or the sham treatment group (n=59). No significant difference in demographic or clinical characteristics between the two groups was found. Prior to the baseline visit, all individuals discontinued all prescription and over-the-counter (OTC) pain medications, herbal supplements, and all other treatments for knee osteoarthritis for a duration of five times the half-life of the medication, and discontinued adjunctive therapies for knee pain for 72 hours. The sham treatment used a sham cryoneurolysis device that did not produce any freezing and had no therapeutic effect. After cryoneurolysis or sham treatment was administered, individuals were assessed at eight follow-up visits (Day 1, Day 7, Day 30, Day 60, Day 90, and Day 120; Days 150 and 180 were included if there was a continued effect reported at the previous visit as determined by WOMAC pain subscale score). “Compared to the sham group, patients who received active treatment had a statistically significant greater change from baseline in the WOMAC pain subscale score at Day 30 (p=0.0004), Day 60 (p=0.0176), and Day 90 (p=0.0061)” (Radnovich, 2017). While the evaluators focus their discussion of the results on the statistical significance in these self-reported outcomes, it should be noted that the least squares (LS) mean absolute differences are small. For example, the LS mean absolute difference from sham (95% confidence interval [CI]) for the WOMAC pain subscale score at Day 30 (primary endpoint) was −7.12 (−11.01 to −3.22). No significant difference in WOMAC pain response rate was noted at Day 120 and beyond. There was a significant difference found between the two groups in the WOMAC physical function and stiffness subscales at Day 30 (p=0.0012; p=0.0060), but not at later follow-up points. Also, a significant difference was noted in VAS responders when comparing the two groups at Day 30 (p=0.0124). “There were no statistically significant differences in [VAS] response rates between the groups at Day 60 (p=0.180), Day 90 (p=0.400), and Day 120 (p=0.5060)” . Use of medications taken for knee pain during the treatment phase of the study was recorded 33 times in 15 (8.3%) individuals (10 [8.3%] active, 5 [8.4%] sham), and use of medications taken for pain other than knee pain was recorded 52 times in 48 (26.6%) individuals (32 [26.4%] active, 16 [27.1%] sham). Out of 243 recorded adverse events, 84 were deemed possibly or probably related to the cryoneurolysis device. All adverse events were mild to moderate except for 1 severe adverse event, which was altered sensation. There were 4 serious adverse events reported, which were all determined to be unrelated to the cryoneurolysis device. While individuals in this study were blinded, the evaluators noted that individuals began to accurately guess their assigned group over time, which could have affected self-reported outcomes and resulted in biased results. Cryoneurolysis for the treatment of knee osteoarthritis resulted in significant outcomes in this study; however, more controlled studies are needed with comparisons to standard pain treatments to validate these findings.

In 2023, Nemecek published a retrospective cohort study of 24 individuals who underwent cryoneurolysis for refractory peripheral mononeuropathy. To be included in the study, individuals needed to have neuropathic pain attributable to a specific peripheral nerve, lack of response to non-invasive therapy, and to experience at least 50% pain relief after two prognostic pain blocks (lidocaine and ropivacaine, respectively). The cohort had a mean pain score of 5.8 (SD, 1.8) before the intervention, using a 10-point numerical rating scale (NRS) to measure pain. Mean NRS scores were 3.4 (SD [standard deviation], 2.6) 1 month after the intervention, 5.4 (SD, 2.1) 3 months after the intervention and 5.5 (SD, 2.0) 6 months after the intervention. Ten participants died before the 3-month follow-up for reasons related to their underlying disease and unrelated to treatment. This study found a short-term benefit associated with treatment, but the benefit dissipated by 3 months. The lack of a control group prevents firm conclusions about the relative effect of cryoneurolysis compared to other pain treatments. The loss of more than 40% of the cohort raises the possibility that results for those lost to follow up, if known, may have significantly affected the results.

The American Society of Anesthesiologists (ASA) Task Force on Chronic Pain Management and the American Society of Regional Anesthesia and Pain Medicine published Practice Guidelines for Chronic Pain Management in 2010. These guidelines include cryoneurolysis and cryoablation in the discussion section; however, the recommendations only include cryoablation for the treatment of peripheral nerve pain and do not address cryoneurolysis (ASA, 2010). The American Academy of Orthopedic Surgeons (AAOS)’s evidence-based clinical practice guideline on the surgical management of osteoarthritis of the knee noted that cryotherapy is one of the interventions that were considered but not recommended (AAOS, 2013). Currently, no major authoritative organizations have published recommendations for the use of cryoneurolysis as a treatment for peripheral nerve pain.

Cryoneurolysis has been proposed for a variety of pain indications including shoulder, hip, and knee pain. Most peer-reviewed evidence on cryoneurolysis focuses on peripheral nerve pain associated with osteoarthritis of the knee. Additional proposed indications include pediatric use following thoracotomy surgery. Evidence published for these other indications consists primarily of small, single-center, retrospective case series and chart reviews with few trial participants.

Pain Control During and After Chest Surgery

Cha and colleagues (2021) conducted a systematic review of observational studies that evaluated the efficacy of intercostal cryoneurolysis as an analgesic adjunct for chest wall pain, specifically addressing the applicability of intercostal cryoneurolysis for pain control after chest wall trauma. Twenty-three studies including 570 individuals undergoing cryoneurolysis met eligibility criteria for quantitative analysis. Five subgroups of participants treated with intercostal cryoneurolysis were identified: pectus excavatum (nine studies); thoracotomy (eight studies); post-thoracotomy pain syndrome (three studies); malignant chest wall pain (two studies); and traumatic rib fractures (one study). The authors concluded that overall low-quality evidence supported intercostal cryoneurolysis as an analgesic adjunct for chest wall pain, and further prospective studies are needed to improve the quality of evidence supporting cryoneurolysis for postoperative pain management compared to other pain treatments. The Cha study did not focus on minimally invasive procedures.

Several randomized controlled trials (RCTs) have compared pain control with and without cyroanalgesia in individuals undergoing minimally invasive chest surgery. Lau and colleagues (2021) evaluated the impact of cryoanalgesia on post-operative outcomes in adults undergoing minimally invasive thoracotomy heart valve surgery (Mini-HVS). The study randomized individuals on a 3:1 basis to cryoanalgesia (n=65) or standard pain management (n=19). Although the stated purpose of the study was “to determine whether intraoperative intercostal cryo nerve block in conjunction with standard of care provided superior analgesic efficacy in patients undergoing Mini-HVS compared to standard-of-care”, the primary study outcome was forced expiratory volume in 1 second (FEV1) in liters (L) at 48 hours post-surgery. Statistical planning for the study included an assumption that 20% improvement in FEV1 would represent a clinically effective change. The planning further estimated that 75 participants would be needed in the cryoanalgesia arm and 25 in the standard care arm to detect a 20% difference in FEV1 with 94% power. The study’s enrollment was less than these targets. A total of 62 of the 84 participants (74%) completed the 48-hour FEV1 assessment. In this group, the average 48-hour FEV1 was higher in the cryoanalgesia group (1.20 L ± 0.46) than the standard care group (0.93 ± 0.43 L). This difference was statistically significant (p=0.02), however the confidence intervals for the two groups showed considerable overlap. This may reflect the fact that this study did not enroll as many participants as their statistical plan required. Pain scores measured by a VAS were secondary outcomes. Mean VAS scores did not differ significantly between groups at 48 hours (p=0.70) or at other time points up to 120 hours post-surgery.

In 2024, Weksler and colleagues published a randomized controlled trial (RCT) evaluating pain control after intercostal nerve block with or without cryoanalgesia in 103 individuals scheduled for a minimally invasive thoracic procedure. There were 51 individuals in the cryoanalgesia group and 51 in a standard care group. In the cryoanalgesia group, 5 to 6 intercostal nerves were ablated. The AtriCure Cryosphere probe was used for cryoanalgesia. The primary study outcome was the amount of narcotics taken during the hospital stay post-operation and the first 2 weeks post-discharge. The researchers found no statistically significant difference between groups in post-operative hospital stay narcotic use in morphine milligram equivalent (MME, 38.4 mg in the cryoanalgesia group versus 44.9 mg in the standard care group, p=0.468). Moreover, there was no statistically significant difference in narcotic use during the first 2 weeks post-discharge (95.2 mg in the cryoanalgesia group versus 108.8 mg in the standard care group). There was also no significant difference between groups in the mean amount of narcotics used during surgery (15 mg MME in the cryoanalgesia group and 15 mg in the standard care group, p=0.903).

Rim and colleagues (2024) compared pain control after intercostal nerve block with or without cryoanalgesia in adolescents ages 10 to 20 years old who received minimally invasive repair of pectus excavatum (MIRPE). There were 24 participants in each group. Due to the additional time required for the cryoanalgesia procedure, the mean operative time was significantly longer in this group (159 minutes) than the standard care group (126 minutes), p=0.0011. The primary outcome measure for postoperative pain was determined by a 10-point VAS at several intervals up to 72 hours after surgery. Pain was rated in both resting (VAS-R) and dynamic (VAS-D) states. At 12 hours, the mean VAS-R score at the anterior chest wall was 4.79 in the cryoanalgesia group and 6.58 in the standard care group (p=0.0001), and the corresponding mean VAS-D scores were 6.17 and 7.83, respectively (p=0.0005). Scores decreased over time but remained over 4 in the cryoanalgsia group until 48 to 72 hours. The authors stated that the results were “less favorable than expected because the VAS was greater than 4 (moderate pain) although after a day or two, it decreased to lower levels (VAS <4) in the cryo group” and concluded that “considering its extra invasiveness and instrumentation, a routine cryoanalgesia procedure for pectus surgery is yet to be determined.”

Spasticity

Cryoneurolysis of peripheral nerves has been proposed as a treatment for spasticity. Use of cryoneurolysis for this indication has been reported in several case reports (Herzog, 2023; Scobie, 2021; Winston, 2019) and one case series (Winston, 2023). No RCTs or controlled observational studies have evaluated cryoneurolysis for the treatment of spasticity.

Winston (2023) included 113 individuals treated for spasticity with cryoneurolysis. The individuals were enrolled in one of three ongoing clinical trials. A total of 59 individuals were enrolled in an upper limb trial, 43 were in a tibial nerve trial and 11 were in a bilateral obturator trial. The analysis focused on any adverse effects related to cryoneurolysis treatment. Adverse events were reported in 3 of 113 individuals (3%). These included a local skin infection (n=1) and bruising or swelling (n=2). All three events resolved by the 1-month follow-up. Nine treatments resulted in reports of nerve pain or dysesthesia; symptoms lasted up to 1 month in 3 individuals, 2 months in 2 individuals and 3 months in 3 individuals; 1 participant reported foot pain beyond 3 months and numbness at their 6-month follow-up. No participant withdrew from their clinical trial due to adverse events. Four individuals died during follow-up; all deaths were due to their underlying medical condition. Spasticity outcomes were not reported. The results of this case series do not support conclusions about the relative effects of cryoneurolysis on spasticity compared to commonly used treatments such as antispasticity medications, nerve blocks, or rhizotomy.

Cryoneurolysis, also referred to as cryoanalgesia, creates a temporary nerve block through application of extreme cold to the selected treatment site. Cryoneurolysis used as a temporary nerve block is also sometimes called cryoablation.

There are several cryogenic devices, which is the U.S. Food and Drug Administration (FDA) identification for devices using cryoneurolysis technology, such as the iovera° System (Myoscience, Inc., Fremont, CA), that have received FDA 510k clearance to administer cryoneurolysis for this indication (FDA, 2018; FDA, 2019). The device uses cryogenic fluid to cool the cryoneurolysis probe, which is introduced percutaneously at the treatment site. Once the probe is under the skin, a localized cold zone is generated and it creates lesions in nervous tissue producing a temporary nerve block for up to 90 days. Cryoneurolysis is used to treat disorders that can cause peripheral nerve pain. Some of these disorders include diabetes, peripheral vascular disease, and autoimmune diseases. Treatment for peripheral nerve pain can be accomplished through medical or surgical management.

Cryosurgical techniques to temporarily block peripheral nerves also can be used to relieve pain during chest procedures. The Cryophere^™ and cryoICE cryoablation probe (AtriCure, Mason, OH) was cleared by the FDA in March, 2020 for use in adults and adolescents at least 12 years of age. The device is intended to temporarily block pain during by ablating intercostal nerves.

Cryoneurolysis can also be used to treat spasticity. Spasticity is a condition in which certain muscles are continuously contracted, causing stiffness or tightness, and resist being stretched. Thus, the condition can interfere with normal movement, gait and speech. Spasticity is caused by damage to the brain and spinal cord and can occur in individuals with spinal injury and conditions such as cerebral palsy and multiple sclerosis. Current treatments for spasticity include medications, physical therapy, botulinum toxin injections and, in severe cases, surgery. (AANS, 2024).

Cryoablation: A minimally invasive procedure that uses extremely cold temperatures to selectively destroy nerve endings to create a block that stops the conduction of pain.

Cryoneurolysis: A surgical procedure that produces lesions in peripheral nervous tissue through application of extreme cold. This process creates a temporary blocking of nerve pain.

Intercostal: Situated between the ribs.

Osteoarthritis: A degenerative condition of the joints that causes destruction of the tissue in the joints that absorbs shock and allows proper movement.

Peripheral nervous system: The collection of nerves and ganglia outside the brain and spinal cord that connects the central nervous system to the rest of the body.

The following codes for treatments and procedures applicable to this document are included below for informational purposes. Inclusion or exclusion of a procedure, diagnosis or device code(s) does not constitute or imply member coverage or provider reimbursement policy. Please refer to the member's contract benefits in effect at the time of service to determine coverage or non-coverage of these services as it applies to an individual member.

When services are Investigational and Not Medically Necessary:
For the following procedure codes, or when the code describes a procedure indicated in the Position Statement section as investigational and not medically necessary.

Peer Reviewed Publications:

1. Cazzato RL, Garnon J, Ramamurthy N, et al. Percutaneous MR-guided cryoablation of Morton's neuroma: Rationale and technical details after the first 20 patients. Cardiovasc Intervent Radiol. 2016; 39(10):1491-1498.
2. Cha PI, Min JG, Patil A, et al. Efficacy of intercostal cryoneurolysis as an analgesic adjunct for chest wall pain after surgery or trauma: systematic review. Trauma Surg Acute Care Open. 2021; 6(1):e000690.
3. Dasa V, Lensing G, Parsons M, et al. Percutaneous freezing of sensory nerves prior to total knee arthroplasty. Knee. 2016; 23(3):523-528.
4. Friedman T, Richman D, Adler R. Sonographically guided cryoneurolysis: preliminary experience and clinical outcomes. J Ultrasound Med. 2012; 31(12):2025-2034.
5. Graves CE, Idowu O, Lee S, et al. Intraoperative cryoanalgesia for managing pain after the Nuss procedure. J Pediatric Surg. 2017; 52 (6):920-924.
6. Herzog S, David R, Speirs A et al. A case report illustrating the combined use of cryoneurolysis and percutaneous needle tenotomy in the treatment of longstanding spastic shoulder contractures after stroke. Arch Rehabil Res Clin Transl. 2023; 5(3):100285.
7. Ilfeld BM, Finneran JJ. Cryoneurolysis and percutaneous peripheral nerve stimulation to treat acute pain. Anesthesiology. 2020; 133(5):1127-1149.
8. Ilfeld BM, Finneran JJ, Swisher MW, et al. Preoperative ultrasound-guided percutaneous cryoneurolysis for the treatment of pain after mastectomy: A randomized, participant- and observer-masked, sham-controlled study. Anesthesiology. 2022; 137(5):529-542.
9. Ilfeld BM, Smith CR, Turan A, et al. Ultrasound-guided percutaneous cryoneurolysis to treat chronic postamputation phantom limb pain: A multicenter randomized controlled trial. Anesthesiology. 2023; 138(1):82-97.
10. Lau WC, Shannon FL, Bolling SF et al. Intercostal cryo nerve block in minimally invasive cardiac surgery: The prospective randomized FROST Trial. Pain Ther. 2021; 10(2):1579-1592.
11. Mihalko WM, Kerkhof AL, Ford MC, et al. Cryoneurolysis before total knee arthroplasty in patients with severe osteoarthritis for reduction of postoperative pain and opioid use in a single-center randomized controlled trial. J Arthroplasty. 2021; 36(5):1590-1598.
12. Nemecek Z, Sturm C, Rauen AC et al. Ultrasound-controlled cryoneurolysis for peripheral mononeuropathies: a retrospective cohort study. Pain Manag. 2023; 13(6):363-372.
13. Radnovich R, Scott D, Patel AT, et al. Cryoneurolysis to treat the pain and symptoms of knee osteoarthritis: a multicenter, randomized, double-blind, sham-controlled trial. Osteoarthritis Cartilage. 2017; 25(8):1247-1256.
14. Rim GM, Kim HK, Koo JM, et al. A randomized controlled trial of cryoanalgesia for pain management following pectus excavatum repair: a single-center, single-blind, parallel design study. Eur J Pediatr Surg. 2024; 34(4):338-345.
15. Scobie J, Winston P. Case report: Perspective of a caregiver on functional outcomes following bilateral lateral pectoral nerve cryoneurotomy to treat spasticity in a pediatric patient with cerebral palsy. Front Rehabil Sci. 2021; 2:719054.
16. Swisher MW, Ball ST, Gonzales FB, et al. A randomized controlled pilot study using ultrasound-guided percutaneous cryoneurolysis of the infrapatellar branch of the saphenous nerve for analgesia following total knee arthroplasty. Pain Ther. 2022; 11(4):1299-1307.
17. Tanaka A. Al-Rstum Z, Leonard SD, et al. Intraoperative intercostals nerve cryoanalgesia improves pain control after descending and thoracoabdominal aortic aneurysm repairs. Ann Thorac Surg. 2020; 109(1):249-254.
18. Weksler B, Maxwell C, Drake L, et al. A randomized study of cryoablation of intercostal nerves in patients undergoing minimally invasive thoracic surgery. J Thorac Cardiovasc Surg. 2024 Nov 9:S0022-5223(24)01026-2.
19. Winston P, MacRae F, Rajapakshe S, et al. Analysis of adverse effects of cryoneurolysis for the treatment of spasticity. Am J Phys Med Rehabil. 2023; 102(11):1008-1013.
20. Winston P, Mills PB, Reebye R, et al. Cryoneurotomy as a percutaneous mini-invasive therapy for the treatment of the spastic limb: Case Presentation, Review of the literature, and proposed approach for use. Arch Rehabil Res Clin Transl. 2019; 1(3-4):100030.
21. Yoon JH, Grechushkin V, Chaudhry A, et al. Cryoneurolysis in patients with refractory chronic peripheral neuropathic pain. J Vasc Interv Radiol. 2016; 27(2):239-243.

Government Agency, Medical Society, and Other Authoritative Publications:

1. American Academy of Orthopaedic Surgeons (AAOS). Treatment of osteoarthritis of the knee. Evidence-Based Guidelines, 2nd ed. Adopted by the American Academy of Orthopaedic Surgeons Board of Directors, May 18, 2013. Rosemont, IL: AAOS; 2013.
2. American Association of Neurological Surgeons (AANS). Spasticity. Available at https://www.aans.org/Patients/Neurosurgical-Conditions-and-Treatments/Spasticity. Accessed on December 10, 2024.
3. American Society of Anesthesiologists (ASA). Practice guidelines for chronic pain management: an updated report by the American Society of Anesthesiologists Task Force on Chronic Pain Management and the American Society of Regional Anesthesia and Pain Medicine. Anesthesiology. 2010; 112(4):810-833.
4. Barrett SL, Nickerson DS, Elison P, et al. The Association of Extremity Nerve Surgeons. Clinical Practice Guidelines 2014. Available at: http://www.aens.us/images/aens/AENSGuidelinesFinal-12082014.pdf. Accessed on December 10, 2024.
5. Kolasinski SL, Neogi T, Hochberg MC, et al. 2019 American College of Rheumatology/Arthritis Foundation Guideline for the Management of Osteoarthritis of the Hand, Hip, and Knee. Arthritis Rheumatol. 2020; 72(2):220-233.
6. Thomas JL, Blitch EL 4th, Chaney DM, et al. Clinical Practice Guideline Forefoot Disorders Panel. Diagnosis and treatment of forefoot disorders. Section 3. Morton's intermetatarsal neuroma. J Foot Ankle Surg. 2009; 48(2):251-256.
7. Thomson CE, Gibson JNA, Martin D. Interventions for the treatment of Morton's neuroma. Cochrane Database of Syst Rev. 2004; 3(CD003118).
8. U.S. Food and Drug Administration 510(k) Premarket Notification Database. AtriCure CryoICE cryo-ablation probe (Cryo2), AtriCure CryoICE CryoSPHERE cryoablation probe (CryoS, CryoS-L) 510(k) Summary. No. K200697. December 23, 2020. Available at: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?id=K200697. Accessed on December 11, 2024.
9. U.S. Food and Drug Administration 510(k) Premarket Notification Database. iovera° system 510(k) Summary. No. K173763. February 28, 2018. Available at: https://www.accessdata.fda.gov/cdrh_docs/pdf17/K173763.pdf. Accessed on December 11, 2024.
10. U.S. Food and Drug Administration Code of Federal Regulations. Title 21 Food and Drugs. Sec. 882.4250. Rockville, MD: FDA. April 1, 2019. Available at: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfcfr/cfrsearch.cfm?fr=882.4250. Accessed on December 11, 2024.

Cryoanalgesia
CryoICE
CryoSphere 
iovera° system

The use of specific product names is illustrative only. It is not intended to be a recommendation of one product over another, and is not intended to represent a complete listing of all products available.

Federal and State law, as well as contract language, including definitions and specific contract provisions/exclusions, take precedence over Coverage Guidelines and must be considered first in determining eligibility for coverage. The member’s contract benefits in effect on the date that services are rendered must be used. Coverage Guidelines, which addresses medical efficacy, should be considered before utilizing medical opinion in adjudication. Medical technology is constantly evolving, and we reserve the right to review and update Coverage Guidelines periodically.

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