DoctorThe Food and Drug Administration granted 31 spine- and orthopedic-related medical device clearances in July.

InstrumentsThe Food and Drug Administration granted 11 spine-related device clearances in June.

Collegeville, Pa.-based Synergy Biomedical received FDA clearance for its BioSphere Putty for bone grafts.
Aliso Viejo, Calif.-based Vertos Medical has closed a $23 million round of Series E financing to fund the U.S. commercial expansion and European launch of its mild procedure for lumbar spinal stenosis.
Sunrise, Fla.-based OrthoSensor received FDA 510(k) clearance for its VERASENSE knee system, an instrument system for implant position during total knee replacements.
SurgeonThe Food and Drug Administration granted 15 spine-related medical device clearances in May.
Blue Belt Technologies received 510(k) clearance from the U.S. Food and Drug Administration for its STRIDE Unicondylar Knee implant.
Spinal Elements, based in Carlsbad, Calif., has licensed a portfolio of patents for accessing the lumbar spine and placing implants from a lateral approach.
Santa Clara, Calif.-based Benvenue Medical completed the yearlong patient follow-up phase in the clinical trial of its Kiva vertebral compression fracture treatment.
Surgical GloveThe Food and Drug Administration granted 35 orthopedic- and spine-focused 510(k) clearances in April.
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