510(k) K161753 ยท KTT Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component
Hoffman LRF System
| Applicant | Stryker GmbH, Mahwah NJ, US |
| Decision | Substantially Equivalent, Nov 15, 2016 |
| Received | Jun 24, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K161753
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.