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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.
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