510(k) K920800 ยท HRX Arthroscope
INTEGRATED ENDOSCOPY SYSTEM 1000
| Applicant | Biomet, Inc., Warsaw IN, US |
| Decision | Substantially Equivalent, Jun 30, 1992 |
| Received | Feb 21, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K920800
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| May 26, 2016 | Biomet, Inc. Various trauma and sports medicine instruments and implants.
Arthroscope. Terminated |
HRX | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.