Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K760001Substantially Equivalent

Arch Support (Arch Aid)

Zimmer GmbH, Walker MI / Traditional, Substantially Equivalent

K760001 is the FDA 510(k) clearance record for ARCH SUPPORT (ARCH AID), cleared for Zimmer, Inc. on . FDA records list 872 510(k) clearances for Zimmer, Inc., from to . As of , FDA records show no recalls naming K760001.

Clearance record

Decision date
Received
(61 days to decision)
Review panel
Unknown
Applicant
Zimmer, Inc. 4221 Richmond Rd., NW, Walker MI
Third party review
No