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FDA 510(k) Application Details - K102019
Device Classification Name
Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented
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510(K) Number
K102019
Device Name
Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented
Applicant
HOWMEDICA OSTEONICS
325 Corporate Drive
Mahwah, NJ 07430 US
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Contact
KAREN ARIEMMA
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Regulation Number
888.3358
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Classification Product Code
LPH
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More FDA Info for this Product Code
Date Received
07/19/2010
Decision Date
03/03/2011
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
OR - Orthopedic
Review Advisory Committee
OR - Orthopedic
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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