510(k) K072879 ยท HRX Arthroscope
INNERVUE DIAGNOSTIC SCOPE SYSTEM
| Applicant | Biomet Orthopedics, Inc., Warsaw IN, US |
| Decision | Substantially Equivalent, Jan 14, 2008 |
| Received | Oct 9, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K072879
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Mar 7, 2011 | Biomet, Inc. Biomet INNERVUE DISPOSABLE SCOPE KIT 1.2MM, PRODUCT NUMBER 922140, STERILE Terminated |
HRX | None listed |
| Mar 7, 2011 | Biomet, Inc. Biomet INNERVUE DISPOSABLE SCOPE KIT 1.2MM WITH CANNULA SET, PRODUCT NUMBER 922141, STERILE Terminated |
HRX | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.