510(k) K130954 ยท HWC Screw, Fixation, Bone
ARS SCREW; SLANT SCREW
| Applicant | Advanced Interventional Technology, LLC, Derwood MD, US |
| Decision | Substantially Equivalent, May 31, 2013 |
| Received | Apr 5, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K130954
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.