| Primary Device ID | 00813426020503 |
| NIH Device Record Key | fac4f807-3375-446f-bbee-786a88ac6cd5 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Nevro |
| Version Model Number | ACCK7200 |
| Catalog Number | ACCK7200 |
| Company DUNS | 926599155 |
| Company Name | NEVRO CORP. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | true |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Phone | 9502510005 |
| info@nevro.com | |
| Phone | 9502510005 |
| info@nevro.com | |
| Phone | 9502510005 |
| info@nevro.com | |
| Phone | 9502510005 |
| info@nevro.com | |
| Phone | 9502510005 |
| info@nevro.com | |
| Phone | 9502510005 |
| info@nevro.com | |
| Phone | 9502510005 |
| info@nevro.com | |
| Phone | 9502510005 |
| info@nevro.com | |
| Phone | 9502510005 |
| info@nevro.com | |
| Phone | 9502510005 |
| info@nevro.com | |
| Phone | 9502510005 |
| info@nevro.com | |
| Phone | 9502510005 |
| info@nevro.com | |
| Phone | 9502510005 |
| info@nevro.com | |
| Phone | 9502510005 |
| info@nevro.com | |
| Phone | 9502510005 |
| info@nevro.com | |
| Phone | 9502510005 |
| info@nevro.com | |
| Phone | 9502510005 |
| info@nevro.com | |
| Phone | 9502510005 |
| info@nevro.com | |
| Phone | 9502510005 |
| info@nevro.com | |
| Phone | 9502510005 |
| info@nevro.com | |
| Phone | 9502510005 |
| info@nevro.com | |
| Phone | 9502510005 |
| info@nevro.com | |
| Phone | 9502510005 |
| info@nevro.com | |
| Phone | 9502510005 |
| info@nevro.com | |
| Phone | 9502510005 |
| info@nevro.com | |
| Phone | 9502510005 |
| info@nevro.com | |
| Phone | 9502510005 |
| info@nevro.com | |
| Phone | 9502510005 |
| info@nevro.com | |
| Phone | 9502510005 |
| info@nevro.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00813426020503 [Primary] |
| LGW | Stimulator, Spinal-Cord, Totally Implanted For Pain Relief |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2020-01-22 |
| Device Publish Date | 2018-01-08 |
| 00813426020510 | Senza II |
| 00813426020503 | IPG2000 Template Kit |
| 00813426020411 | Passing Elevator Accessory Tool |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() NEVRO 85794051 not registered Dead/Abandoned |
Jones, Ivan, Carrington Means 2012-12-04 |
![]() NEVRO 85254957 not registered Dead/Abandoned |
Nevro Corp. 2011-03-01 |
![]() NEVRO 85066215 not registered Dead/Abandoned |
Nevro Corp. 2010-06-18 |
![]() NEVRO 85066213 4280176 Live/Registered |
Nevro Corp. 2010-06-18 |
![]() NEVRO 85066206 not registered Dead/Abandoned |
Nevro Corp. 2010-06-18 |
![]() NEVRO 85066199 4280175 Live/Registered |
Nevro Corp. 2010-06-18 |
![]() NEVRO 77165563 3923415 Live/Registered |
NEVRO CORP. 2007-04-25 |