Surpass LEAD2005-90B

GUDID 00813426020640

Surpass-C Surgical Lead Kit, 90cm

NEVRO CORP.

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 ID00813426020640
NIH Device Record Key98f5eb79-13ff-4eca-b325-e13daa0cdc5d
Commercial Distribution StatusIn Commercial Distribution
Brand NameSurpass
Version Model NumberLEAD2005-90B
Catalog NumberLEAD2005-90B
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 Perscriptiontrue
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

Device Identifiers

Device Issuing AgencyDevice ID
GS100813426020640 [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 StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-04-16
Device Publish Date2020-04-08

On-Brand Devices [Surpass]

00813426020640Surpass-C Surgical Lead Kit, 90cm
00813426020633Surpass-C Surgical Lead Kit, 50cm
00813426020589Surpass-C Surgical Lead Kit, 70cm

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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