# K262098: EnHAnce PEEK Bunion System

- Pathway: 510(k) (Special)
- Applicant: Nvision Biomedical Technologies
- Decided: Sep 18, 2026 after 88 days
- Product code: HRS (Plate, Fixation, Bone)
- Device class: 2
- Regulation: 21 CFR 888.3030
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 20 generations back to K962616 (1996). 242 ancestors in all.
No later device cites it as a predicate yet.
0 of 243 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K253718: enHAnce PEEK Bunion System, Nvision Biomedical Technologies, Inc. (2026) Summary page 5.
- K241014: Biomet Kirschner Wires (K-Wires), Biomet, Inc. (2024) Summary page 5.

## Indications for use
The enHAnce PEEK Bunion System is intended for fixation of osteotomies and corrective procedures of the hallux and associated disorders, such as hallux valgus.

Source page: https://510kreport.com/device/K262098
Methodology: https://510kreport.com/methodology