Surpass™ LEAD3005-90B

GUDID 00813426020473

Surgical Lead Kit, 90cm

NEVRO CORP.

Analgesic spinal cord electrical stimulation system Analgesic spinal cord electrical stimulation system Implantable lumbar neuromuscular electrical stimulation system lead Implantable lumbar neuromuscular electrical stimulation system lead Implantable lumbar neuromuscular electrical stimulation system lead Implantable lumbar neuromuscular electrical stimulation system lead Implantable lumbar neuromuscular electrical stimulation system lead Implantable lumbar neuromuscular electrical stimulation system lead Implantable lumbar neuromuscular electrical stimulation system lead Implantable lumbar neuromuscular electrical stimulation system lead Implantable lumbar neuromuscular electrical stimulation system lead Implantable lumbar neuromuscular electrical stimulation system lead Implantable lumbar neuromuscular electrical stimulation system lead Implantable lumbar neuromuscular electrical stimulation system lead Implantable lumbar neuromuscular electrical stimulation system lead Implantable lumbar neuromuscular electrical stimulation system lead Implantable lumbar neuromuscular electrical stimulation system lead Implantable lumbar neuromuscular electrical stimulation system lead Spinal cord/peripheral nerve implantable analgesic electrical stimulation system lead Spinal cord/peripheral nerve implantable analgesic electrical stimulation system lead Spinal cord/peripheral nerve implantable analgesic electrical stimulation system lead Spinal cord/peripheral nerve implantable analgesic electrical stimulation system lead Spinal cord/peripheral nerve implantable analgesic electrical stimulation system lead Spinal cord/peripheral nerve implantable analgesic electrical stimulation system lead Spinal cord/peripheral nerve implantable analgesic electrical stimulation system lead Spinal cord/peripheral nerve implantable analgesic electrical stimulation system lead Spinal cord/peripheral nerve implantable analgesic electrical stimulation system lead Spinal cord/peripheral nerve implantable analgesic electrical stimulation system lead Spinal cord/peripheral nerve implantable analgesic electrical stimulation system lead Spinal cord/peripheral nerve implantable analgesic electrical stimulation system lead, wired connection Spinal cord/peripheral nerve implantable analgesic electrical stimulation system lead, wired connection Spinal cord/peripheral nerve implantable analgesic electrical stimulation system lead, wired connection Spinal cord/peripheral nerve implantable analgesic electrical stimulation system lead, wired connection Spinal cord/peripheral nerve implantable analgesic electrical stimulation system lead, wired connection Spinal cord/peripheral nerve implantable analgesic electrical stimulation system lead, wired connection Spinal cord/peripheral nerve implantable analgesic electrical stimulation system lead, wired connection Spinal cord/peripheral nerve implantable analgesic electrical stimulation system lead, wired connection Spinal cord/peripheral nerve implantable analgesic electrical stimulation system lead, wired connection Spinal cord/peripheral nerve implantable analgesic electrical stimulation system lead, wired connection Spinal cord/peripheral nerve implantable analgesic electrical stimulation system lead, wired connection Spinal cord/peripheral nerve implantable analgesic electrical stimulation system lead, wired connection Spinal cord/peripheral nerve implantable analgesic electrical stimulation system lead, wired connection Spinal cord/peripheral nerve implantable analgesic electrical stimulation system lead, wired connection
Primary Device ID00813426020473
NIH Device Record Keye631818b-e93f-42fb-b52d-c9b04fb6dd53
Commercial Distribution StatusIn Commercial Distribution
Brand NameSurpass™
Version Model NumberLEAD3005-90B
Catalog NumberLEAD3005-90B
Company DUNS926599155
Company NameNEVRO CORP.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusMR Unsafe
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Customer Support Contacts

Phone650-251-0005
Emailinfo@nevro.com
Phone650-251-0005
Emailinfo@nevro.com
Phone650-251-0005
Emailinfo@nevro.com
Phone650-251-0005
Emailinfo@nevro.com
Phone650-251-0005
Emailinfo@nevro.com
Phone650-251-0005
Emailinfo@nevro.com
Phone650-251-0005
Emailinfo@nevro.com
Phone650-251-0005
Emailinfo@nevro.com
Phone650-251-0005
Emailinfo@nevro.com
Phone650-251-0005
Emailinfo@nevro.com
Phone650-251-0005
Emailinfo@nevro.com
Phone650-251-0005
Emailinfo@nevro.com
Phone650-251-0005
Emailinfo@nevro.com
Phone650-251-0005
Emailinfo@nevro.com
Phone650-251-0005
Emailinfo@nevro.com
Phone650-251-0005
Emailinfo@nevro.com
Phone650-251-0005
Emailinfo@nevro.com
Phone650-251-0005
Emailinfo@nevro.com
Phone650-251-0005
Emailinfo@nevro.com
Phone650-251-0005
Emailinfo@nevro.com
Phone650-251-0005
Emailinfo@nevro.com
Phone650-251-0005
Emailinfo@nevro.com
Phone650-251-0005
Emailinfo@nevro.com
Phone650-251-0005
Emailinfo@nevro.com
Phone650-251-0005
Emailinfo@nevro.com
Phone650-251-0005
Emailinfo@nevro.com
Phone650-251-0005
Emailinfo@nevro.com
Phone650-251-0005
Emailinfo@nevro.com
Phone650-251-0005
Emailinfo@nevro.com
Phone650-251-0005
Emailinfo@nevro.com
Phone650-251-0005
Emailinfo@nevro.com
Phone650-251-0005
Emailinfo@nevro.com
Phone650-251-0005
Emailinfo@nevro.com
Phone650-251-0005
Emailinfo@nevro.com
Phone650-251-0005
Emailinfo@nevro.com
Phone650-251-0005
Emailinfo@nevro.com
Phone650-251-0005
Emailinfo@nevro.com
Phone650-251-0005
Emailinfo@nevro.com
Phone650-251-0005
Emailinfo@nevro.com
Phone650-251-0005
Emailinfo@nevro.com
Phone650-251-0005
Emailinfo@nevro.com
Phone650-251-0005
Emailinfo@nevro.com
Phone650-251-0005
Emailinfo@nevro.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100813426020473 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

LGWStimulator, Spinal-Cord, Totally Implanted For Pain Relief

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2016-12-31

On-Brand Devices [Surpass™]

00813426020480Surgical Lead Kit, 70cm
00813426020473Surgical Lead Kit, 90cm
00813426020466Surgical Lead Kit, 50cm

Trademark Results [Surpass]

Mark Image

Registration | Serial
Company
Trademark
Application Date
SURPASS
SURPASS
98244700 not registered Live/Pending
Chongqing Sipasi E-Commerce Co., Ltd.
2023-10-28
SURPASS
SURPASS
98042379 not registered Live/Pending
Surpass Industry Co., Ltd.
2023-06-14
SURPASS
SURPASS
97926504 not registered Live/Pending
Shenzhen Muxing Zhichuang Technology Co., Ltd.
2023-05-08
SURPASS
SURPASS
97712793 not registered Live/Pending
CSL Behring L.L.C.
2022-12-12
SURPASS
SURPASS
97637693 not registered Live/Pending
Ray Beyond Behavioral Corp.
2022-10-18
SURPASS
SURPASS
97637687 not registered Live/Pending
Ray Beyond Behavioral Corp.
2022-10-18
SURPASS
SURPASS
97637670 not registered Live/Pending
Ray Beyond Behavioral Corp.
2022-10-18
SURPASS
SURPASS
97637660 not registered Live/Pending
Ray Beyond Behavioral Corp.
2022-10-18
SURPASS
SURPASS
97529366 not registered Live/Pending
BK Technologies, Inc.
2022-08-01
SURPASS
SURPASS
97403839 not registered Live/Pending
Standard Textile Co., Inc.
2022-05-10
SURPASS
SURPASS
97079290 not registered Live/Pending
WUXI YONGHONG TECHNOLOGY CO., LTD.
2021-10-18
SURPASS
SURPASS
88699201 not registered Live/Pending
USLBG
2019-11-20

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