Ventris Medical Gains 510(k) for Backpack Bone Graft Containment
Backpack is designed for optimization of cell proliferation and bone formation and is used in orthopedic and spinal fusion procedures....
Backpack is designed for optimization of cell proliferation and bone formation and is used in orthopedic and spinal fusion procedures....
FDA approved an expansion to its Phase I/II clinical program to include three spinal fusion indications and tripling the number...
Three of the company’s MagnetOs bone graft formulations are already indicated for use beyond spine procedures....
LDGraft is a combination product that delivers recombinant human bone morphogenetic protein-2 through a biodegradable polymer....
The FDA clearance allows NovaBone Putty to be used in the intervertebral disc space alongside FDA-cleared interbody fusion devices....
CITREPORE is a synthetic bioactive bone void filler composed of patented CITREGEN biomaterial technology....
At six months post-grafting surgery with NVDX3, x-rays demonstrate that 90% of patients have reached, or are steadily progressing towards,...
The designation covers use of a drug/device combination product to treat degenerative disc disease with transforaminal lumbar interbody fusion....
Results support integration of antibiotic-eluting bone substitute materials, like CERAMENT G and CERAMENT V, into treatment guidelines for orthopedic infections....
i-FACTOR is now approved for single-level ACDF with an allograft bone ring, or with a PEEK, titanium alloy or PEEK/titanium...
As a guest member you get access to more articles and videos every month.
We’ll send a recovery link to your email.
Return to Homepage