FDA UDI In Commercial Distribution 🇺🇸 United States

Nevro®

DI: 00813426020251 · Model: ACCK5300 · NEVRO CORP.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Nevro®
Primary DI
00813426020251
Version / Model
ACCK5300
Catalog Number
ACCK5300
Company Name
NEVRO CORP.
Labeler DUNS
926599155
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-05-21
Public Version
5
Public Version Date
2022-11-09
Public Version Status
Update
Public Device Record Key
7adb7459-ef9e-4715-b1e7-707fe405426a

Device Description

N300 Lead Anchor Kit

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
MR Conditional
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
LGW Stimulator, Spinal-Cord, Totally Implanted For Pain Relief

GMDN Terms

Code Name
45612 Soft-tissue/mesh anchor, non-bioabsorbable

Identifiers

Type ID
Primary 00813426020251

Customer Contacts

Phone
6502510005

Premarket Submissions

Submission Number Supplement Number
P130022 000