Baxter Gains FDA Clearance for Bone Graft Substitute
Baxter International received FDA 510(k) clearance for its Actifuse Flow bone graft substitute. ...
Baxter International received FDA 510(k) clearance for its Actifuse Flow bone graft substitute. ...
Histogenics' Phase III clinical trial of NeoCart® tissue engineered implant did not meet the primary endpoint of a statistically significant improvement in pain...
CartiHeal announced successful enrollment of the first Belgian patient in the Agili-C IDE pivotal study....
CartiHeal announced successful enrollment of the first two U.S. patients in the Agili-C IDE pivotal study....
BONESUPPORT received regulatory approval from Health Canada for CERAMENT® G gentamicin-eluting injectable ceramic bone graft substitute....
Cerapedics enrolled the first patients in an IDE clinical trial evaluating P-15L Bone Graft vs. autograft in TLIF....
Wright Medical commenced U.S. launch of the PROstep Minimally Invasive Surgery System and AUGMENT® Injectable Bone Graft....
Kuros Biosciences announced the first commercial uses of MagnetOs bone graft substitute in the U.S. and U.K....
Lipogems received FDA 510(k) clearance to market a Microfragmented Adipose Tissue Transplant system for use in orthopaedic and arthroscopic procedures. ...
In the Phase III 16-02 clinical trial of Anika Therapeutics' CINGAL, statistically significant results in pain reduction were not demonstrated...
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