510(k) K180573 ยท HWC Screw, Fixation, Bone
Responsive Arthroscopy Interference Screw System
| Applicant | Responsive Arthroscopy, LLC, Minneapolis MN, US |
| Decision | Substantially Equivalent, Nov 23, 2018 |
| Received | Mar 5, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K180573
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.