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FDA 510(k) Application Details - K962541
Device Classification Name
Prosthesis, Hip, Acetabular Mesh
More FDA Info for this Device
510(K) Number
K962541
Device Name
Prosthesis, Hip, Acetabular Mesh
Applicant
SMITH & NEPHEW RICHARDS, INC.
1450 E. BROOKS RD.
MEMPHIS, TN 38116 US
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Contact
THOMAS L GRAIG
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Regulation Number
878.3300
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Classification Product Code
JDJ
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More FDA Info for this Product Code
Date Received
06/28/1996
Decision Date
09/17/1996
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
SU - General & Plastic Surgery
Review Advisory Committee
OR - Orthopedic
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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