FDA 510(k) Applications Submitted by InNeuroCo, Inc

FDA 510(k) Number Submission Date Device Name Applicant
K190338 02/14/2019 046 Zenith Flex InNeuroCo, Inc
K161262 05/05/2016 Super Distal Access (SDA) INNEUROCO, INC
K171672 06/06/2017 065 Zenith, 074 Zenith InNeuroCo, Inc
K172468 08/15/2017 091 Long Sheath, 70 cm, 091 Long Sheath, 80 cm, 091 Long Sheath, 90 cm InNeuroCo, Inc
K173709 12/04/2017 Zenith Support, 95 cm, Zenith Support, 105 cm, Zenith Support, 115 cm InNeuroCo, Inc


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