510(k) K800800 ยท HTG Prosthesis, Knee, Hemi-, Patellar Resurfacing, Uncemented
PATELLAR COMPONENT FOR LUBINUS PATELLAR
| Applicant | Waldemar Link GmbH & Co. KG, Mchenry IL, US |
| Decision | Substantially Equivalent, Apr 21, 1980 |
| Received | Apr 10, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K800800
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.