FDA 510(k) Applications for Medical Device Product Code "BXM"
(Stimulator, Nerve, Ac-Powered)

FDA 510(k) Number Applicant Device Name Decision Date
K870662 LIFE-TECH INTL., INC. MODEL SKCK STERILE KNOB COVER KIT 10/28/1987
K013215 NUVASIVE, INC. MODIFIED INS-1 INTRAOPERATIVE NERVE SURVEILLANCE SYSTEM 10/16/2001
K002677 NUVASIVE, INC. NUVASIVE INS-1 INTRAOPERATIVE NERVE SURVEILLANCE SYSTEM 11/13/2000
K921498 VERMONT MEDICAL, INC. VER MED A10011 PNS DUAL ELEMENT ELECTRODE 06/09/1993


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