510(k) K120359 ยท HRS Plate, Fixation, Bone
ORTHOLOC 3DI HALLUX SYSTEM
| Applicant | Wrightmedicaltechnologyinc, Arlington TN, US |
| Decision | Substantially Equivalent, May 3, 2012 |
| Received | Feb 6, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K120359
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Apr 26, 2023 | Wright Medical Technology, Inc. stryker ORTHOLOC 3Di Fusion Plate MTP Right, REF 58A220RT, bone stabilization and fixation Open, Classified |
HRS | None listed |
| Apr 26, 2023 | Wright Medical Technology, Inc. stryker ORTHOLOC 3Di Fusion Plate MTP Right, REF 58A221RT, bone stabilization and fixation Open, Classified |
HRS | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.