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

FREEMAN-SAMUELSON MARK II PRESS-FIT TOTAL KNEE REP

K Number: K853730 · Decision Feb 18, 1986
Classifications
1
FEI Numbers
32
Registration Numbers
32
Same Product Code
13
Applicant Total
25
Review Days
165

Basic Information

Device Name
FREEMAN-SAMUELSON MARK II PRESS-FIT TOTAL KNEE REP
K Number
K853730
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3560
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Applicant
PROTEK, INC.
Date Received
September 6, 1985
Decision Date
February 18, 1986
Product Code
MBV
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
MBV Prosthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uhmwpe, Pegged, Cemented, Polymer/Metal/Polymer

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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. →