510(k) K980609 ยท HSB Rod, Fixation, Intramedullary And Accessories
SEGMENTAL DEFECT REPLACEMENT SYSTEM
| Applicant | Metagen, LLC, San Diego CA, US |
| Decision | Substantially Equivalent, May 18, 1998 |
| Received | Feb 17, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K980609
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.