510(k) K882322 ยท JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer
CONTINUUM KNEE SYSTEM (CKS)
| Applicant | Buckman Co., Inc., Martinez CA, US |
| Decision | Substantially Equivalent for Some Indications, Feb 8, 1989 |
| Received | Jun 6, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K882322
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.