510(k) K812053

SILASTIC HEMI WRIST IMPLANT H.P. (RAD.) by Dow Corning Corp. Healthcare Industries Materials — Product Code KXE

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 18, 1981
Date Received
July 21, 1981
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Prosthesis, Wrist, Hemi-, Ulnar
Device Class
Class II
Regulation Number
888.3810
Review Panel
OR
Submission Type