510(k) K102429 ยท HRS Plate, Fixation, Bone
ORTHOLOC 3DI ANKLE PLATING SYSTEM, ORTHOLOC BONE SCREW
| Applicant | Wrightmedicaltechnologyinc, Arlington TN, US |
| Decision | Substantially Equivalent, Nov 23, 2010 |
| Received | Aug 25, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K102429
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Nov 8, 2016 | Wright Medical Technology, Inc. ORTHOLOC 3DI PLT SYS STERILE, LOCKING SCREW, 3.5 x 38mm Sterile, Part Number 58S03538 Terminated |
HWC | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.