510(k) K870141 ยท HWC Screw, Fixation, Bone
URESIL T-SYSTEM BONE SCREWS
| Applicant | Uresil Corp., Skokie IL, US |
| Decision | Substantially Equivalent, Feb 3, 1987 |
| Received | Jan 13, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K870141
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.