510(k) K940913 ยท HRX Arthroscope
SPINE-TECH LAPAROSCOPIC INSTRUMENTATION SYSTEM
| Applicant | Spine-Tech, Inc., Minneapolis MN, US |
| Decision | Substantially Equivalent, Oct 4, 1994 |
| Received | Feb 25, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K940913
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.