M.W.P. WRIST PROSTHESIS— 510(k) K872502

Substantially Equivalent

Protek, Inc.

FDA 510(k) clearance K872502 for M.W.P. WRIST PROSTHESIS, Substantially Equivalent on 1987-07-23. Applicant: Protek, Inc.. Device class: 2.

Clearance details

Applicant: Protek, Inc.
Product code: Code KWM
Device class: Class 2
Regulation: 21 CFR 888.3800
Advisory panel: Orthopedic
Date received: 1987-06-24
Decision date: 1987-07-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Indianapolis, IN, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code KWM

K880156 — VOLZ TOTAL WRIST PROSTHESIS1988-02-17
K803031 — LAURE WRIST IMPLANT1982-06-29
K800602 — TALEISNIK TOTAL WRIST PROSTHESIS1980-08-27
K801157 — WEBER-MAYO WRIST1980-08-04
K790774 — LODA WRIST PROSTHESIS1979-08-03

More clearances from Protek, Inc.

K893785 — ARC-2F ACETABULAR CUP1989-08-09
K893959 — P.S.A. FEMORAL HIP PROSTHESIS1989-07-25
K892059 — FEMORAL HEADS/MODULAR & FIXED W/ TITAN NITRIDE SUR1989-07-19
K883794 — RESUBMITTED CLW ACETABULAR CUP W/SULMESH1989-05-26
K884952 — VARIOUS FEMORAL HIP PROSTHESES W/SELF LOCK CERAMIC1989-05-10

Data sourced from openFDA. This site is unofficial and independent of the FDA.