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FDA 510(k) Applications Submitted by Ad-Tech Medical Instrument Corporation
FDA 510(k) Number
Submission Date
Device Name
Applicant
K223269
10/24/2022
Spencer Probe Depth Electrodes
Ad-Tech Medical Instrument Corporation
K223276
10/24/2022
Anchor Bolts as Accessories to Depth Electrodes
Ad-Tech Medical Instrument Corporation
K170442
02/14/2017
Cranial Drill Bits and Accessories
Ad-Tech Medical Instrument Corporation
K191186
05/03/2019
Subdural Strip/Intraoperative Split Electrode, Subdural Grid/Intraoperative Grid Electrode, Dual-Sided Interhemispheric Subdural Electrode, Multi-Strip and Slit Grid Subdural Electrode, Intraoperative Mapping Grid Subdural Electrode
Ad-Tech Medical Instrument Corporation
K181544
06/12/2018
Anchor Bolt (as an accessory to Depth Electrodes)
Ad-Tech Medical Instrument Corporation
K152547
09/08/2015
DNAP Electrode
Ad-Tech Medical Instrument Corporation
K152769
09/25/2015
FREMAP ELECTRODE
AD-TECH MEDICAL INSTRUMENT CORPORATION
K163355
11/30/2016
Depth Electrodes, Foramen Ovale Depth Eletrodes, Marco-Micro Depth Electrodes, Spencer Probe Depth Electrodes
Ad-Tech Medical Instrument Corporation
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