# Royal Oak Medical Devices

- Location (FDA's records): Bloomfield Hills, MI
- FDA decisions: 2 (2011–2011): 2 510(k) clearances
- Product codes: MAX (1), NKB (1)
- Predicates its devices cite: 11 (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

## Firms whose devices it cites most
- Depuyacromed: 2 (https://510kreport.com/company/depuyacromed)
- Stryker Spine: 1 (https://510kreport.com/company/stryker-spine)
- Depuy Spine, Inc.: 1 (https://510kreport.com/company/depuy-spine)
- Eminent Spine: 1 (https://510kreport.com/company/eminent-spine)
- Spine Smith Partners L.P.: 1 (https://510kreport.com/company/spine-smith-partners)
- Zimmer Spine, Inc.: 1 (https://510kreport.com/company/zimmer-spine)
- Buckman Co., Inc.: 1 (https://510kreport.com/company/buckman)
- Cross Medical Products, Inc.: 1 (https://510kreport.com/company/cross-medical-products)

## Recent decisions
- K110046: Athena Pedicle Screw System (Dec 7, 2011)
- K110177: Helena System (Apr 21, 2011)

Source page: https://510kreport.com/company/royal-oak-medical-devices