Atlas FDA

NeuroPace RNS System

FDA premarket approval P100026/S084 · decided 2020-09-28

Approval details

PMA number
P100026
Supplement
S084
Supplement type
Normal 180 Day Track No User Fee
Supplement reason
Postapproval Study Protocol
Trade name
NeuroPace RNS System
Generic name
Implanted brain stimulator for epilepsy
Applicant
NeuroPace, Inc.
Date received
2020-08-14
Decision date
2020-09-28
Days to decision
45 days
Decision code
APPR
Product code
PFN
Advisory committee
Neurology
Expedited review
No
Location
Mountain View, CA
Statement
Approval to update the protocols and associated data collection and informed consent forms for PAS 2 and PAS 3 due to the current public health emergency.

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510(k) clearances by this applicant

RecordFirmDate
NEUROPACE BURR HOLE COVER (K141368)NeuroPace, Inc.2014-07-11
NEUROPACE BURR HOLE COVER MODEL 8110 (K123163)NeuroPace, Inc.2013-01-18