NeuroPace, Inc. is one of 5120 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
NeuroPace, Inc. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
NeuroPace, Inc. has 2 FDA 510(k) cleared medical devices. Based in Mountaint View, US.
Historical record: 2 cleared submissions from 2013 to 2014. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by NeuroPace, Inc. Filter by specialty or product code using the sidebar.
NeuroPace, Inc. — FDA 510(k) Products and Clearance History
2 devices
Cleared
Jul 11, 2014
NEUROPACE BURR HOLE COVER
Neurology
49d
Cleared
Jan 18, 2013
NEUROPACE BURR HOLE COVER MODEL 8110
Neurology
101d