# Cartiva, Inc.

- Location (FDA's records): Alpharetta, GA
- FDA decisions: 4 (2014–2019): 3 510(k) clearances and 1 original PMA approval
- Product codes: QBO (2), PNW (1), HWC (1)
- Predicates its devices cite: 3 (0 its own); citations of its devices by later devices: 1 (0 its own)
- Recalls linked to its devices: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Wrightmedicaltechnologyinc: 1 (https://510kreport.com/company/wrightmedicaltechnologyinc)
- New Deal, S.A.: 1 (https://510kreport.com/company/new-deal)
- Arthrex, Inc.: 1 (https://510kreport.com/company/arthrex)

## Firms that cite its devices most
- Graham Medical Technologies, LLC (D.B.A.Gramedica): 1 (https://510kreport.com/company/graham-medical-technologies-dbagramedica)

## Its most-cited devices
- K142490: ProxiFuse Hammer Toe Device (2014), cited by 1

## Recent decisions
- K192156: Cartiva SCI instrumentation set (Sep 4, 2019)
- K181348: Cartiva SCI Disposable Instrumentation Set (Jun 20, 2018)
- P150017: Cartiva Synthetic Cartilage Implant (Jul 1, 2016)
- K142490: ProxiFuse Hammer Toe Device (Dec 15, 2014)

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