FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

M.W.P. WRIST PROSTHESIS

K Number: K872502 · Decision Jul 23, 1987
Classifications
1
FEI Numbers
4
Registration Numbers
4
Same Product Code
5
Applicant Total
25
Review Days
29

Basic Information

Device Name
M.W.P. WRIST PROSTHESIS
K Number
K872502
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3800
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Applicant
PROTEK, INC.
Date Received
June 24, 1987
Decision Date
July 23, 1987
Product Code
KWM
Advisory Committee
Orthopedic
Review Advisory Committee
OR
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
KWM Prosthesis, Wrist, Semi-Constrained

Similar 510(k) Clearances

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Other Clearances by PROTEK, INC.

K Number Device Name
K893785 ARC-2F ACETABULAR CUP
K893959 P.S.A. FEMORAL HIP PROSTHESIS
K892059 FEMORAL HEADS/MODULAR & FIXED W/ TITAN NITRIDE SUR
K883794 RESUBMITTED CLW ACETABULAR CUP W/SULMESH
K884952 VARIOUS FEMORAL HIP PROSTHESES W/SELF LOCK CERAMIC
K884889 MODIFIED O.E.C. UNIV. SELF-ALIGNING ACETA. COMP.
K890054 M.E.M. ACETABULAR CUP W/SULMESH FOR CEMENT APPLI.
K884789 NEW JERSEY FEMORAL HIP PROSTHESIS FOR CEMENT APPLI
K884888 MODIFIED NEW JERSEY ACETABULAR COMP. & BONE SCREWS
K882671 SAMUELSON SCREWLOC CUP
Search all 25 clearances from PROTEK, INC. →