510(k) K013672 ยท JEY Plate, Bone
BRUGES DISTRACTION - ANCHORING - OSTEOSYNTHESIS SYSTEM
| Applicant | Azary Technologies, LLC, Huntington CT, US |
| Decision | Substantially Equivalent, Apr 8, 2002 |
| Received | Nov 6, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K013672
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.