# K210665: Nerve Tape

- Pathway: 510(k) (Traditional)
- Applicant: Biocircuit Technologies, Incorporated
- Decided: Jul 15, 2022 after 497 days
- Product code: JXI (Cuff, Nerve)
- Device class: 2
- Regulation: 21 CFR 882.5275
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 5 generations back to K921895 (1992). 13 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 15 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K162741: AxoGuard Nerve Connector, Cook Biotech Incorporated (2016) Summary page 4.
- K132660: Nerve Cuff, Cook Biotech Incorporated (2014) Summary page 4.

## Most influential descendants
- K233533: NerveTape (2024), 0 descendants of its own

## Indications for use
Nerve Tape is indicated for the repair of peripheral nerve discontinuities where gap closure can be achieved by flexion of the extremity.

Source page: https://510kreport.com/device/K210665
Methodology: https://510kreport.com/methodology