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U.S. Department of Health and Human Services

510(k) Premarket Notification

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Device Classification Name prosthesis, hip, semi-constrained, metal/polymer, porous uncemented
510(k) Number K973124
Device Name APR POROUS HA HIP SYSTEM
Applicant
SULZER ORTHOPEDICS, INC.
9900 SPECTRUM DR.
austin,  TX  78717
Applicant Contact lori k holder
Correspondent
SULZER ORTHOPEDICS, INC.
9900 SPECTRUM DR.
austin,  TX  78717
Correspondent Contact lori k holder
Regulation Number888.3358
Classification Product Code
LPH  
Subsequent Product Code
MEH  
Date Received08/20/1997
Decision Date 11/03/1997
Decision substantially equivalent for some indications (SN)
Regulation Medical Specialty Orthopedic
510k Review Panel Orthopedic
summary summary
Type Traditional
Reviewed by Third Party No
Combination Product No
Recalls CDRH Recalls
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