510(k) K032180 ยท JDK Prosthesis, Hip, Cement Restrictor
NUVASIVE CEMENT RESTRICTOR
| Applicant | Nuvasive, Inc., San Diego CA, US |
| Decision | Unknown, Oct 7, 2003 |
| Received | Jul 17, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K032180
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.