# Neucoll, Inc.

- Location (FDA's records): Los Gatos
- FDA decisions: 2 (1993–2001): 1 510(k) clearance and 1 original PMA approval
- Product codes: MBS (1), MQV (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 7 (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
- Medtronic Sofamor Danek: 1 (https://510kreport.com/company/medtronic-sofamor-danek)
- R and D Medical, LLC: 1 (https://510kreport.com/company/r-and-d-medical)
- Collagen Matrix, Inc.: 1 (https://510kreport.com/company/collagen-matrix)
- Depuy Spine, Inc.: 1 (https://510kreport.com/company/depuy-spine)
- Orquest, Inc.: 1 (https://510kreport.com/company/orquest)
- Exactech, Inc.: 1 (https://510kreport.com/company/exactech)
- Baxter Healthcare Corp: 1 (https://510kreport.com/company/baxter-healthcare)

## Its most-cited devices
- K000122: Collagraft Strip Bone Graft Matrix (for Use as a Bone Filler), Model 1X,3X,6X (1,3 or 6 Strips Per Box) (2001), cited by 7

## Recent decisions
- K000122: Collagraft Strip Bone Graft Matrix (for Use as a Bone Filler), Model 1X,3X,6X (1,3 or 6 Strips Per Box) (Sep 20, 2001)
- P900039: Collagraft (TM) Bone Graft Substitute (May 28, 1993)

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