510(k) K034037 ยท HRX Arthroscope
SKY BONE EXPANDER SYSTEM
| Applicant | Disc-O-Tech Medical Technologies, Ltd., Washington DC, US |
| Decision | Substantially Equivalent, Jan 28, 2004 |
| Received | Dec 29, 2003 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K034037
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.