NervAlign Nerve Cuff
FDA 510(k) clearance K202234 · decided 2022-02-10
Clearance details
- K-number
- K202234
- Device name
- NervAlign Nerve Cuff
- Applicant
- Renerve, Ltd.
- Decision
- Substantially Equivalent
- Date received
- 2020-08-07
- Decision date
- 2022-02-10
- Days to decision
- 552 days
- Clearance type
- Traditional
- Product code
- JXI
- Device class
- 2
- Regulation number
- 882.5275
- Medical specialty
- Neurology
- Advisory committee
- Neurology
- Location
- North Melbourne, AU
- Third-party review
- No
- Expedited review
- No
+ Add to Predicate Builder ◉ Watch Renerve
Need this as data, not a web page?
Query all 176,000+ clearances through the Atlas FDA API, or subscribe to weekly change alerts. Self-serve from $29/mo.
Similar devices under this product code
Devices cleared under the same product code - the starting set for predicate research.
Recalls involving this device
No recalls on record reference this clearance.