Surpass™ LEAD3005-90B
GUDID 00813426020473
Surgical Lead Kit, 90cm
NEVRO CORP.
Analgesic spinal cord electrical stimulation system| Primary Device ID | 00813426020473 |
| NIH Device Record Key | e631818b-e93f-42fb-b52d-c9b04fb6dd53 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Surpass™ |
| Version Model Number | LEAD3005-90B |
| Catalog Number | LEAD3005-90B |
| Company DUNS | 926599155 |
| Company Name | NEVRO CORP. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | MR Unsafe |
| 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 | false |
| OTC Over-The-Counter | false |
Customer Support Contacts
| Phone | 650-251-0005 |
| info@nevro.com | |
| Phone | 650-251-0005 |
| info@nevro.com | |
| Phone | 650-251-0005 |
| info@nevro.com | |
| Phone | 650-251-0005 |
| info@nevro.com | |
| Phone | 650-251-0005 |
| info@nevro.com | |
| Phone | 650-251-0005 |
| info@nevro.com | |
| Phone | 650-251-0005 |
| info@nevro.com | |
| Phone | 650-251-0005 |
| info@nevro.com | |
| Phone | 650-251-0005 |
| info@nevro.com | |
| Phone | 650-251-0005 |
| info@nevro.com | |
| Phone | 650-251-0005 |
| info@nevro.com | |
| Phone | 650-251-0005 |
| info@nevro.com | |
| Phone | 650-251-0005 |
| info@nevro.com | |
| Phone | 650-251-0005 |
| info@nevro.com | |
| Phone | 650-251-0005 |
| info@nevro.com | |
| Phone | 650-251-0005 |
| info@nevro.com | |
| Phone | 650-251-0005 |
| info@nevro.com | |
| Phone | 650-251-0005 |
| info@nevro.com | |
| Phone | 650-251-0005 |
| info@nevro.com | |
| Phone | 650-251-0005 |
| info@nevro.com | |
| Phone | 650-251-0005 |
| info@nevro.com | |
| Phone | 650-251-0005 |
| info@nevro.com | |
| Phone | 650-251-0005 |
| info@nevro.com | |
| Phone | 650-251-0005 |
| info@nevro.com | |
| Phone | 650-251-0005 |
| info@nevro.com | |
| Phone | 650-251-0005 |
| info@nevro.com | |
| Phone | 650-251-0005 |
| info@nevro.com | |
| Phone | 650-251-0005 |
| info@nevro.com | |
| Phone | 650-251-0005 |
| info@nevro.com | |
| Phone | 650-251-0005 |
| info@nevro.com | |
| Phone | 650-251-0005 |
| info@nevro.com | |
| Phone | 650-251-0005 |
| info@nevro.com | |
| Phone | 650-251-0005 |
| info@nevro.com | |
| Phone | 650-251-0005 |
| info@nevro.com | |
| Phone | 650-251-0005 |
| info@nevro.com | |
| Phone | 650-251-0005 |
| info@nevro.com | |
| Phone | 650-251-0005 |
| info@nevro.com | |
| Phone | 650-251-0005 |
| info@nevro.com | |
| Phone | 650-251-0005 |
| info@nevro.com | |
| Phone | 650-251-0005 |
| info@nevro.com | |
| Phone | 650-251-0005 |
| info@nevro.com | |
| Phone | 650-251-0005 |
| info@nevro.com | |
| Phone | 650-251-0005 |
| info@nevro.com |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00813426020473 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Approval: P130022
FDA Product Code
| LGW | Stimulator, Spinal-Cord, Totally Implanted For Pain Relief |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | true |
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2016-12-31 |
On-Brand Devices [Surpass™]
| 00813426020480 | Surgical Lead Kit, 70cm |
| 00813426020473 | Surgical Lead Kit, 90cm |
| 00813426020466 | Surgical Lead Kit, 50cm |
Trademark Results [Surpass]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 SURPASS 98244700 not registered Live/Pending |
Chongqing Sipasi E-Commerce Co., Ltd. 2023-10-28 |
 SURPASS 98042379 not registered Live/Pending |
Surpass Industry Co., Ltd. 2023-06-14 |
 SURPASS 97926504 not registered Live/Pending |
Shenzhen Muxing Zhichuang Technology Co., Ltd. 2023-05-08 |
 SURPASS 97712793 not registered Live/Pending |
CSL Behring L.L.C. 2022-12-12 |
 SURPASS 97637693 not registered Live/Pending |
Ray Beyond Behavioral Corp. 2022-10-18 |
 SURPASS 97637687 not registered Live/Pending |
Ray Beyond Behavioral Corp. 2022-10-18 |
 SURPASS 97637670 not registered Live/Pending |
Ray Beyond Behavioral Corp. 2022-10-18 |
 SURPASS 97637660 not registered Live/Pending |
Ray Beyond Behavioral Corp. 2022-10-18 |
 SURPASS 97529366 not registered Live/Pending |
BK Technologies, Inc. 2022-08-01 |
 SURPASS 97403839 not registered Live/Pending |
Standard Textile Co., Inc. 2022-05-10 |
 SURPASS 97079290 not registered Live/Pending |
WUXI YONGHONG TECHNOLOGY CO., LTD. 2021-10-18 |
 SURPASS 88699201 not registered Live/Pending |
USLBG 2019-11-20 |
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.