510(k) K971682 ยท LRN Wire, Surgical
J-FX CERCLAGE SYSTEM
| Applicant | Johnson & Johnson Professionals, Inc., Raynham MA, US |
| Decision | Substantially Equivalent, Jun 27, 1997 |
| Received | May 6, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K971682
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.