510(k) K131820 ยท HRX Arthroscope
AVAMAX VERTEBRAL BALLOON SYSTEM, 8G, AVAMAX VERTEBRAL BALLOON SYSTEM, 10G, AVAMAX VERTEBRAL BALLOON SYSTEM, 11G
| Applicant | Care Fusion, Vernon Hills IL, US |
| Decision | Substantially Equivalent, Oct 4, 2013 |
| Received | Jun 20, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K131820
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.