Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K862752Substantially Equivalent

C.s.m. Hip

Protek, Inc., Indianapolis IN / Traditional, Substantially Equivalent

K862752 is the FDA 510(k) clearance record for C.S.M. HIP, cleared for Protek, Inc. on . FDA records list 25 510(k) clearances for Protek, Inc., from to . As of , FDA records show no recalls naming K862752.

Clearance record

Decision date
Received
(16 days to decision)
Review panel
Unknown
Applicant
Protek, Inc. 5780 W. 71st St., Indianapolis IN
Third party review
No