FDA.reportPublic FDA data

NEVRO CORP.

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30085140293008514029NEVRO CORP.1N2026-01-011800 Bridge Pkwy Redwood City CA US 94065

GUDID Contact Samples#

Sampled from matched GUDID device records for this company; this is not an exhaustive company contact directory.

Source GUDID, Product, Phone table
Source GUDIDProductPhoneEmail
00813426020091Nevro® - Blue S8 Lead Adaptor Kit, 25cm6502510005info@nevro.com
00813426020107Nevro® - Blue M8 Lead Adaptor Kit, 25cm6502510005info@nevro.com
00813426020169Senza® - Senza® Patient Trial Kit6502510005info@nevro.com

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
1190601174853717P130022NEVRO SENZA SPINAL CORD STIMULATION (SCS) SYSTEMLGW2015-05-08

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
LGW12015-05-08

PMA#

Senza Spinal Cord Stimulation (SCS) System, Senza HFX iQ System

2022-12-23

Nevro Corporation1800 Bridge Parkwayredwood City, CA 94065 PMA NumberP130022 Supplement NumberS047 Date Received11/22/2022 Decision Date12/23/2022 Product Code LGW  Advisory Committee Neurology Supplement Type30-day Notice Supplement Reason Process Change -...

Nevro Corp Senza™ Spinal Cord Stimulation (SCS) System

2022-05-13

Nevro Corporation1800 Bridge Parkwayredwood City, CA 94065 PMA NumberP130022 Supplement NumberS046 Date Received04/15/2022 Decision Date05/13/2022 Product Code LGW  Advisory Committee Neurology Supplement Typespecial (immediate Track) Supplement Reason Labe...

GUDID#

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