Breakthrough Device Designation for Infuse Bone Graft
This designation addresses Infuse in a TLIF approach in the treatment of degenerative disease of the lumbosacral spine....
This designation addresses Infuse in a TLIF approach in the treatment of degenerative disease of the lumbosacral spine....
Catalyst nanosynthetic bone graft stimulates the formation of healthy bone tissue in spinal fusion surgeries....
Upon hydration, the graft transforms into a pliable form that can be tailored to meet precise needs of diverse surgical...
Expanded indications for Agilon Moldable and Morpheus Moldable address use in the intervertebral disc space as an autograft extender....
Lipogems completed enrollment in the ARISE I FDA IDE study examining MicroFat vs. corticosteriod injection for the treatment of knee...
The first patient is enrolled in ARISE II, an IDE research study to examine investigational MicroFat vs. saline injection to...
GID BIO completed enrollment for the first of two pivotal Phase III studies to investigate the use of your own...
BONESUPPORT's CERAMENT G is an orthopedic medical device combination matrix comprising a resorbable synthetic bone graft substitute and the antibiotic...
FDA granted 510(k) marketing clearance in the intervertebral disc space for Amplify Synthetic Bone Graft Putty....
HydroPutty bone graft features hydrophilic carriers designed to absorb fluids such as bone marrow aspirate, blood or saline....
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