510(k) K070179 ยท FCG Biopsy Needle
TROKABONE, TROKABONE STERNAL
| Applicant | PAJUNK GmbH Medizintechnologie, Geisingen, DE |
| Decision | Substantially Equivalent, Mar 7, 2007 |
| Received | Jan 19, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K070179
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.