510(k) K210016 ยท HRS Plate, Fixation, Bone
Integra DigiFuse Cannulated Intramedullary Fusion System,Integra Total Foot System,Integra CAPTURE Screw System & Integra Ti6 Internal Fixation System,Subtalar MBA System,MetaSurg Subtalar Implant,NewDeal BOLD Screw,NewDeal HALLU Lock Plate System,NewDeal HALLU Plates,QWIX Positioning Screw,SPIN Sna
| Applicant | Integra LifeSciences Corporation, Austin TX, US |
| Decision | Substantially Equivalent, Jul 27, 2021 |
| Received | Jan 4, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K210016
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.