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FDA 510(k) Application Details - K053293
Device Classification Name
Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented
More FDA Info for this Device
510(K) Number
K053293
Device Name
Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented
Applicant
ORTHO DEVELOPMENT CORP.
12187 SOUTH BUSINESS PARK DR.
DRAPER, UT 84020 US
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Contact
WILLIAM J GRIFFIN
Other 510(k) Applications for this Contact
Regulation Number
888.3358
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Classification Product Code
LPH
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
11/25/2005
Decision Date
02/16/2006
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
OR - Orthopedic
Review Advisory Committee
OR - Orthopedic
Statement / Summary / Purged Status
Statement
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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