FDA 510(k) Applications Submitted by CARL KNOBLOCH

FDA 510(k) Number	Submission Date	Device Name	Applicant
K010322	02/02/2001	ISKD (INTRAMEDULLARY SKELETAL KINETIC DISTRACTOR)	ORTHODYNE, INC.
K050473	02/24/2005	RBK PATELLA FEMORAL KNEE	GLOBAL ORTHOPAEDIC TECHNOLOGY, USA, INC.
K051721	06/27/2005	GLOBAL RESURFACING UNICOMPARTMENTAL KNEE SYSTEM	GLOBAL ORTHOPAEDIC TECHNOLOGY, USA, INC.
K051959	07/18/2005	NV CORMED SOLAS SPINAL SYSTEM	NV CORMED
K051965	07/20/2005	OSTEOBRIDGE IDSF INTRAMEDULLARY DIAPHYSEAL SEGMENTAL DEFECT FIXATION ROD SYSTEM	MERETE MEDICAL GMBH
K033351	10/20/2003	GLOBAL RESURFACING UNICOMPARTMENTAL (GRU) KNEE	GLOBAL ORTHOPAEDIC TECHNOLOGY, USA, INC.
K043411	12/10/2004	RESOFIX BIOABSORBABLE EXPANSION BOLT	RESOFIX, INC.