510(k) K022615 ยท JDK Prosthesis, Hip, Cement Restrictor
CENTERPULSE, SPINE-TECH DIVISION CEMENT RESTRICTOR
| Applicant | Centerpulse Spine-Tech, Inc., Minneapolis MN, US |
| Decision | Unknown, Oct 29, 2002 |
| Received | Aug 7, 2002 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K022615
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.