# Epic Extremity, LLC

- Location (FDA's records): Cranberry Twp, PA
- FDA decisions: 5 (2016–2019): 5 510(k) clearances
- Product codes: HRS (3), HWC (2)
- 510(k) review time since 2016: median 87 days, against 122 for FDA's reviews in the same codes and years (4 of 5 faster)
- Predicates its devices cite: 10 (3 its own); citations of its devices by later devices: 4 (3 its own)
- Recalls linked to its devices: 2 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Wrightmedicaltechnologyinc: 5 (https://510kreport.com/company/wrightmedicaltechnologyinc)
- Darco International, Inc.: 1 (https://510kreport.com/company/darco-international)
- Aap Implantate AG: 1 (https://510kreport.com/company/aap-implantate)

## Firms that cite its devices most
- Exactech, Inc.: 1 (https://510kreport.com/company/exactech)

## Its most-cited devices
- K153340: Epic Extremity Plate System (2016), cited by 2
- K172441: EPIC Extremity Fracture Plate System (2017), cited by 1
- K153333: Epic Extremity Cannulated Screw System (2016), cited by 1

## Recent decisions
- K182991: EPIC Extremity Fusion Plate System (Feb 13, 2019)
- K172441: EPIC Extremity Fracture Plate System (Nov 6, 2017)
- K163038: EPIC Extremity Snap-Off Screw (Feb 28, 2017)
- K153340: Epic Extremity Plate System (Feb 9, 2016)
- K153333: Epic Extremity Cannulated Screw System (Jan 19, 2016)

Source page: https://510kreport.com/company/epic-extremity