510(k) K131620 ยท HWC Screw, Fixation, Bone
JONES-FX FRACTURE SYSTEM
| Applicant | Instratek, Inc., Houston TX, US |
| Decision | Substantially Equivalent, Jul 25, 2013 |
| Received | Jun 3, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K131620
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.