Atlas FDA

NeuroPace RNS System

FDA premarket approval P100026/S083 · decided 2020-07-14

Approval details

PMA number
P100026
Supplement
S083
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
NeuroPace RNS System
Generic name
Implanted brain stimulator for epilepsy
Applicant
NeuroPace, Inc.
Date received
2020-07-10
Decision date
2020-07-14
Days to decision
4 days
Decision code
OK30
Product code
PFN
Advisory committee
Neurology
Expedited review
No
Location
Mountain View, CA
Statement
Use of an alternate sub-tier supplier to cut the polyester mesh, which is subsequently fully encapsulated within the NeuroPace Cortical Strip Leads during manufacturing.

Class III intelligence, same tools

PMAs share the API, exports and alerts with 510(k) data - watch an applicant and hear about every approval.

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