Atlas FDA

NeuroPace® RNS® System

FDA premarket approval P100026/S088 · decided 2022-01-18

Approval details

PMA number
P100026
Supplement
S088
Supplement type
Real-Time Process
Supplement reason
Labeling Change - Indications/instructions/shelf life/tradename
Trade name
NeuroPace® RNS® System
Generic name
Implanted brain stimulator for epilepsy
Applicant
NeuroPace, Inc.
Date received
2021-10-28
Decision date
2022-01-18
Days to decision
82 days
Decision code
APPR
Product code
PFN
Advisory committee
Neurology
Expedited review
No
Location
Mountain View, CA
Statement
Approval to modify the labeling for the NeuroPace® RNS® Neurostimulator model RNS-320 to provide updated estimates for battery longevity.

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