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FDA 510(k) Applications Submitted by CAROL J FREASIER
FDA 510(k) Number
Submission Date
Device Name
Applicant
K000321
02/02/2000
HEMISPHERE MODULAR CUP SYSTEM
ORTHO DEVELOPMENT CORP.
K020383
02/05/2002
ORTHO DEVELOPMENT BALANCED KNEE TIBIAL TRAY PEGGED
ORTHO DEVELOPMENT CORP.
K020649
02/28/2002
ENVISION ANTERIOR CERVICAL PLATE SYSTEM
ORTHO DEVELOPMENT CORP.
K990986
03/24/1999
CONTOUR SPINAL SYSTEM
ORTHO DEVELOPMENT CORP.
K971581
04/30/1997
HEMISPHERE CEMENTED CUP
ORTHO DEVELOPMENT CORP.
K982389
07/09/1998
ODC B2 BIPOLAR CUP
ORTHO DEVELOPMENT CORP.
K012129
07/09/2001
ORTHO DEVELOPMENT ORION-I EMF SYSTEM
ORTHO DEVELOPMENT CORP.
K994370
12/27/1999
ORTHO DEVELOPMENT BALANCED KNEE SYSTEM
ORTHO DEVELOPMENT CORP.
K970675
02/24/1997
HEADLOC CERAMIC HEAD
ORTHO DEVELOPMENT CORP.
K971426
04/17/1997
HEADLOC CERAMIC HEAD
ORTHO DEVELOPMENT CORP.
K971435
04/18/1997
HEADLOC CERAMIC FEMORAL HEADS
ORTHO DEVELOPMENT CORP.
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