510(k) K943873 ยท LXH Orthopedic Manual Surgical Instrument
ORTHOMET ANATOMICALLY GUIDED CARPAL TUNNEL RELEASE SY
| Applicant | Orthomet, Inc., Minneapolis MN, US |
| Decision | Substantially Equivalent, Apr 26, 1995 |
| Received | Aug 9, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K943873
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.