510(k) K983814 ยท JDO Device, Fixation, Proximal Femoral, Implant
GOTFRIED PERCUTANEOUS COMPRESSION PLATING SYSTEM
| Applicant | Efratgo, Ltd. HI Tech Bio-Surgical, Washington DC, US |
| Decision | Substantially Equivalent, Jan 14, 1999 |
| Received | Oct 28, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K983814
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.