510(k) K101939 ยท HSB Rod, Fixation, Intramedullary And Accessories
OSTEOBRIDGE IKA INTRAMEDULLARY KNEE ARTHRODESIS ROD FIXATION SYSTEM
| Applicant | Merete Medical GmbH, Rye NY, US |
| Decision | Substantially Equivalent, Oct 7, 2010 |
| Received | Jul 12, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K101939
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Sep 18, 2020 | Merete Medical GmbH OsteoBridge Intremedullary Knee Arthrodesis (IKA) nails Terminated |
HSB | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.