# Cohort Medical Products Group, Inc.

- Location (FDA's records): Hayward, CA
- FDA decisions: 5 (1994–1997): 5 510(k) clearances
- Product codes: HWC (2), HRX (1), HXB (1), KWQ (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K964975: Cohort Discectomy Systems (CDS) (Feb 24, 1997)
- K950011: Cohort (TM) Anterior Plate System (Aps) (Nov 6, 1995)
- K943804: Bone Screw (Dec 8, 1994)
- K943472: Cohort Avb Retractor System (Oct 20, 1994)
- K943474: Cannulated Bone Screw (Oct 14, 1994)

Source page: https://510kreport.com/company/cohort-medical-products-group