510(k) K150871 ยท HWC Screw, Fixation, Bone
ForeFoot STP System
| Applicant | Tornier, Inc., Medina OH, US |
| Decision | Substantially Equivalent, Aug 4, 2015 |
| Received | Apr 1, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K150871
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.