510(k) K093820 ยท HWC Screw, Fixation, Bone
SUBFIX ARTHROEREISIS IMPLANT, MODELS SUT0065, SUT0080, SUT0090, SUT0100, SUT0115
| Applicant | Memometal Technologies, Bruz, FR |
| Decision | Substantially Equivalent, May 19, 2010 |
| Received | Dec 14, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K093820
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.