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U.S. Department of Health and Human Services

510(k) Premarket Notification

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Device Classification Name prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer/metal/polymer
510(k) Number K002335
Device Name NATURAL-KNEE II SYSTEM-DURASUL TIBIAL INSERT AND DURASUL ALL-POLY PATELLA
Applicant
SULZER ORTHOPEDICS, INC.
9900 SPECTRUM DR.
austin,  TX  78717
Applicant Contact mitchell dhority
Correspondent
SULZER ORTHOPEDICS, INC.
9900 SPECTRUM DR.
austin,  TX  78717
Correspondent Contact mitchell dhority
Regulation Number888.3560
Classification Product Code
JWH  
Date Received08/01/2000
Decision Date 10/25/2000
Decision substantially equivalent (SESE)
Regulation Medical Specialty Orthopedic
510k Review Panel Orthopedic
Type Traditional
Reviewed by Third Party No
Combination Product No
Recalls CDRH Recalls
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