510(k) K141041 ยท OTD Endovascular Suturing System
APTUS HELI-FX ANCILLARY ENDOANCHOR CASSETTE
| Applicant | Aptus Endosystems, Sunnyvale CA, US |
| Decision | Substantially Equivalent, May 16, 2014 |
| Received | Apr 23, 2014 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K141041
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.