510(k) K032358 ยท HRX Arthroscope
B-TWIN BONE EXPANDER SYSTEM (B-TWIN BE SYSTEM)
| Applicant | Disc-O-Tech Medical Technologies, Ltd., Washington DC, US |
| Decision | Substantially Equivalent, Dec 17, 2003 |
| Received | Jul 30, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K032358
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.