# Accelerated Innovation, LLC

- Location (FDA's records): Clifton, NJ
- FDA decisions: 7 (2008–2008): 7 510(k) clearances
- Product codes: KWY (1), KWQ (1), KRR (1), JDI (1), JWH (1), LPH (1), MNH (1)
- Predicates its devices cite: 20 (0 its own); citations of its devices by later devices: 18 (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
- Stelkast Company: 9 (https://510kreport.com/company/stelkast)
- Vertebron, Inc.: 8 (https://510kreport.com/company/vertebron)
- Osteonics Corp.: 2 (https://510kreport.com/company/osteonics)
- Zimmer, Inc.: 1 (https://510kreport.com/company/zimmer)

## Firms that cite its devices most
- Arthrex, Inc.: 10 (https://510kreport.com/company/arthrex)
- Cardo Medical Corp.: 6 (https://510kreport.com/company/cardo-medical)
- Total Joint Orthopedics, Inc.: 1 (https://510kreport.com/company/total-joint-orthopedics)
- Altus Partners, LLC: 1 (https://510kreport.com/company/altus-partners)

## Its most-cited devices
- K081127: Accin Total Knee System (2008), cited by 9
- K073120: Accin Patellofemoral System (2008), cited by 4
- K073068: Accin Hip System (2008), cited by 3
- K073530: Accin Anterior Cervical Plate System (2008), cited by 2

## Recent decisions
- K081127: Accin Total Knee System (Oct 17, 2008)
- K080647: Accin Bipolar Head System (Jul 8, 2008)
- K080539: Accin Unipolar Head System (Jun 2, 2008)
- K073120: Accin Patellofemoral System (Feb 29, 2008)
- K073531: Accin Pedicle Screw System (Feb 4, 2008)
- K073530: Accin Anterior Cervical Plate System (Jan 31, 2008)
- K073068: Accin Hip System (Jan 10, 2008)

Source page: https://510kreport.com/company/accelerated-innovation