510(k) K951268 ยท HRX Arthroscope
SPINE-TECH MODIFIED LAPAROSCOPIC SPINAL FUSION INSTRUMENT SYSTEM
| Applicant | Spine-Tech, Inc., Minneapolis MN, US |
| Decision | Substantially Equivalent, Jul 31, 1995 |
| Received | Mar 21, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K951268
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.