Atlas FDA

NeuroPace RNS System

FDA premarket approval P100026/S051 · decided 2018-01-09

Approval details

PMA number
P100026
Supplement
S051
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
2017-12-11
Decision date
2018-01-09
Days to decision
29 days
Decision code
OK30
Product code
PFN
Advisory committee
Neurology
Expedited review
No
Location
Mountain View, CA
Statement
Two changes to occur at NeuroPaces approved battery supplier: 1) to replace an aging Lid Assembly Machine (LAM) welding equipment with equivalent equipment; and 2) to change the sourcing location of the battery ferrules (same supplier, different location).

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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