FDA 510(k) Applications Submitted by CAROL 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.