510(k) K982222 ยท HWC Screw, Fixation, Bone
SYNTHES (USA) DISTAL FEMUR PLATE (DFP) SYSTEM
| Applicant | Synthes (Usa), Paoli PA, US |
| Decision | Substantially Equivalent, Jul 29, 1998 |
| Received | Jun 24, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K982222
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.