510(k) K962644 ยท JDO Device, Fixation, Proximal Femoral, Implant
VIGOR COMPRESSION HIP SCREW SYSTEM
| Applicant | Deutschland Surgical, Inc., Dallas TX, US |
| Decision | Substantially Equivalent, Sep 6, 1996 |
| Received | Jul 8, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K962644
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.