NovaBone Putty Cleared for Use in Interbody Fusion
The FDA clearance allows NovaBone Putty to be used in the intervertebral disc space alongside FDA-cleared interbody fusion devices....
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...
The trial is evaluating SB-01, the first intradiscal pharmacologic treatment to enter Phase III studies for the treatment of chronic...
NanoBone is a next-generation osteoinductive bone graft comprising nanostructured hydroxyapatite for remodelling bone....
The first patient has been treated in the Phase I/II OASIS Trial, a study evaluating the safety and effectiveness of...
COPAL G+V antibiotic-loaded PMMA bone cement contains gentamicin and vancomycin to support periprosthetic joint infection treatment....
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