510(k) K081240 ยท HRX Arthroscope
TIGER DISCECTOMY DEVICE
| Applicant | Spinal Devices, LLC, Apple Valley MN, US |
| Decision | Substantially Equivalent, Feb 27, 2009 |
| Received | May 1, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K081240
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.