Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K870156Substantially Equivalent

Flexmedics Nitinol Mammory Wire

Flexmedics, Minneapolis MN / Traditional, Substantially Equivalent

K870156 is the FDA 510(k) clearance record for FLEXMEDICS NITINOL MAMMORY WIRE, cleared for Flexmedics on . FDA records list 20 510(k) clearances for Flexmedics, from to . As of , FDA records show no recalls naming K870156.

Clearance record

Decision date
Received
(42 days to decision)
Review panel
Unknown
Applicant
Flexmedics Section 12, Minneapolis MN
Third party review
No