# Pectofix, Inc.

- Location (FDA's records): Metuchen, NJ
- FDA decisions: 2 (2000–2001): 2 510(k) clearances
- Product codes: JDQ (2)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 1 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- KLS-Martin L.P.: 1 (https://510kreport.com/company/kls-martin)

## Its most-cited devices
- K000694: Pectofix Dynamic Sternal Fixation System (DSF) (2000), cited by 1

## Recent decisions
- K003951: Pectofix Sternal Repair Wire (Mar 21, 2001)
- K000694: Pectofix Dynamic Sternal Fixation System (DSF) (May 11, 2000)

Source page: https://510kreport.com/company/pectofix