510(k) K130334 ยท KTT Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component
HOFFMANN LRF (LIMB RECONSTRUCTION FRAME SYSTEM)
| Applicant | Stryker Trauma AG, Mahwah NJ, US |
| Decision | Substantially Equivalent, May 3, 2013 |
| Received | Feb 11, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K130334
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.