# Cedar Surgical, Inc.

- Location (FDA's records): Minnetonka, MN
- FDA decisions: 17 (1985–1987): 17 510(k) clearances
- Product codes: HAO (2), GAD (2), HTJ (1), LWG (1), GZT (1), HXR (1), GDG (1), GEG (1), HWA (1), HBE (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
- K873692: Raylor (TM) Drill Stop (Dec 17, 1987)
- K872281: Raylor Fusion Funnel (Nov 2, 1987)
- K873690: Cedar (TM) Pelvic Cushion (Oct 26, 1987)
- K873691: Cedar (TM) Retractor Ring (Sep 28, 1987)
- K864425: Raylor (TM) Dissecting Hook (Dec 12, 1986)
- K864426: Raylor (TM) Depth Gauge (Nov 26, 1986)
- K864421: Raylor (TM) Periosteal Elevators (Nov 26, 1986)
- K864424: Raylor (TM) Protective Retractor (Nov 26, 1986)

Source page: https://510kreport.com/company/cedar-surgical