510(k) K193451 ยท HWC Screw, Fixation, Bone
Titanium Interference Screws
| Applicant | Biomet, Inc., Warsaw IN, US |
| Decision | Substantially Equivalent, Feb 24, 2020 |
| Received | Dec 13, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K193451
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.