# Orthopaedic Device Corp.

- Location (FDA's records): Allendale, NJ
- FDA decisions: 4 (1986–1987): 4 510(k) clearances
- Product codes: KWY (1), KWL (1), JDL (1), KTT (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
- K870234: P.T.H. Metal-Backed Acetabular Cup (Mar 20, 1987)
- K862460: Femoral Hemi-Hip Prosthesis (Oct 6, 1986)
- K863343: Superfixation (TM) (Sep 15, 1986)
- K855228: Femoral Hemi-Hip Prostheses (Feb 11, 1986)

Source page: https://510kreport.com/company/orthopaedic-device