510(k) K032212 ยท HRX Arthroscope
KYPHX DIRECTIONAL INFLATABLE BONE TAMP, MODELS K16A AND K17A
| Applicant | Kyphon, Inc., Sunnyvale CA, US |
| Decision | Substantially Equivalent, Sep 15, 2003 |
| Received | Jul 21, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K032212
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.