Osteotech receives FDA nod for Plexur P
The FDA has cleared Osteotech Inc.’s Plexur P biocomposite for use in spinal applications as a bone void filler and graft extender. Osteotech has already received FDA clearance for Plexur P for use in filling bony voids of the pelvis and extremities. The biocomposite has been used in tibial plateau fractures, tibial osteotomies and foot and ankle procedures. The company aims to immediately offer our Plexur P(TM) product to spine surgeons.
-
Osteotech gets FDA nod for Plexur M(TM) Biocomposite
European Edition Of SAGE Foot and Ankle Specialist To Launch
ApaTech launches Actifuse MIS
ArthroCare Receives FDA Clearance For Parallax Contour Vertebral Augmentation Device
FDA Accepts PMA Application for Augment Bone Graft
