510(k) K982390 ยท KTW Appliance, Fixation, Nail/Blade/Plate Combination, Single Component
CONCISE COMPRESSION HIP SCREW SYSTEM (STERILE)
| Applicant | Wrightmedicaltechnologyinc, Arlington TN, US |
| Decision | Substantially Equivalent, Sep 14, 1998 |
| Received | Jul 9, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K982390
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.