510(k) K102688 ยท KTT Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component
MERETE LOCKING BONE PLATE SYSTEM II
| Applicant | Merete Medical GmbH, Rye NY, US |
| Decision | Substantially Equivalent, Dec 3, 2010 |
| Received | Sep 17, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K102688
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.