FDA Approves Centinel Spine’s Two-Level prodisc L for Total Disc Replacement
The prodisc line now comprises six devices, including an anterior and anterior-lateral approach lumbar disc replacement and four cervical disc...
The prodisc line now comprises six devices, including an anterior and anterior-lateral approach lumbar disc replacement and four cervical disc...
Signus Medizintechnik announced CE Mark approval for the BIG® ST ALIF Cage and JASPIS® ST Cervical Cage, additions to the...
Precision Spine globally launched the Reform® Ti Titanium Pedicle Screw for degenerative and trauma spine procedures....
NuVasive voluntarily issued an Urgent Field Safety Notice in the U.K. and Ireland to address concerns identified by The Medicines and Healthcare Products...
Nexxt Spine received FDA 510(k) clearance of the Nexxt Matrixx® Corpectomy System, and commenced product launch....
Safe Orthopaedics received regulatory approval of SteriSpineâ„¢ PS 2nd Generation in Japan....
OrthoPediatrics was granted FDA 510(k) clearance to expand indications for the RESPONSE™ Scoliosis System to include neuromuscular implants....
AgNovos Healthcare was granted Breakthrough Device Designation by FDA for the AGN1 Local Osteo-enhancement Procedure Small Volume Kit for the treatment of...
Precision Spine launched the Reform POCT (Posterior Occipital Cervical Thoracic) System in the U.S....
The European Patent Office confirmed the strength of certain of Safe Orthopaedics' patents following an opposition procedure by Neo Medical....
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