510(k) K120802 ยท HRS Plate, Fixation, Bone
ORTHOLOC(TM) 3DI LOCKING SCREWS ORTHOLOC(TM) BONE SCREWS
| Applicant | Wrightmedicaltechnologyinc, Arlington TN, US |
| Decision | Substantially Equivalent, Apr 2, 2012 |
| Received | Mar 16, 2012 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K120802
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.