# K233533: NerveTape

- Pathway: 510(k) (Traditional)
- Applicant: Biocircuit Technologies, Inc.
- Decided: Feb 12, 2024 after 102 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: 6 generations back to K921895 (1992). 14 ancestors in all.
No later device cites it as a predicate yet.
0 of 15 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K210665: Nerve Tape, Biocircuit Technologies, Incorporated (2022) Summary page 5.

## Indications for use
NerveTape 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/K233533
Methodology: https://510kreport.com/methodology