Vanta™ AdaptiveStim™

GUDID 00763000849078

INS 977006 VANTA US EMAN CARDIO

MEDTRONIC, INC.

Spinal cord/peripheral nerve implantable analgesic electrical stimulation system pulse generator, implantable
Primary Device ID00763000849078
NIH Device Record Key4535df32-ee66-4ec2-8750-92823f60628f
Commercial Distribution StatusIn Commercial Distribution
Brand NameVanta™ AdaptiveStim™
Version Model Number977006
Company DUNS796986144
Company NameMEDTRONIC, INC.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusMR Conditional
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchfalse
Serial Numbertrue
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100763000849078 [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 Date2024-05-27
Device Publish Date2024-05-19

Devices Manufactured by MEDTRONIC, INC.

20199150004151 - NA2025-04-07 CUSTOM PACK BB10V58R1 10PK SHELBY BPT PG
20199150004311 - NA2025-04-07 CUSTOM PACK BB12P29R 4PK TABLE LNS
00763000959616 - AEX2025-04-04 AEX GENERATOR 40-405-1R REFURB US
20763000651736 - Aortic Punch2025-03-31 Aortic Punch APU425 - 2.5mm punch size
20763000651743 - Aortic Punch2025-03-31 Aortic Punch APU430 - 3.0mm punch size
20763000651750 - Aortic Punch2025-03-31 Aortic Punch APU435 - 3.5mm punch size
20763000651767 - Aortic Punch2025-03-31 Aortic Punch APU440 - 4.0mm punch size
20763000651774 - Aortic Punch2025-03-31 Aortic Punch APU444 - 4.4mm punch size

Trademark Results [Vanta]

Mark Image

Registration | Serial
Company
Trademark
Application Date
VANTA
VANTA
97891810 not registered Live/Pending
Vanta Global, LLC
2023-04-17
VANTA
VANTA
97830784 not registered Live/Pending
Vanta Inc.
2023-03-09
VANTA
VANTA
90144752 not registered Live/Pending
Vanta Inc.
2020-08-28
VANTA
VANTA
90144728 not registered Live/Pending
Vanta Inc.
2020-08-28
VANTA
VANTA
90072563 not registered Live/Pending
Wilbur-Ellis Company LLC
2020-07-24
VANTA
VANTA
88871429 not registered Live/Pending
Vantage Group LLC
2020-04-14
VANTA
VANTA
88681390 not registered Live/Pending
Vanta Inc.
2019-11-05
VANTA
VANTA
88420363 not registered Live/Pending
Medtronic, Inc.
2019-05-08
VANTA
VANTA
87717029 5534145 Live/Registered
Olympus Corporation
2017-12-12
VANTA
VANTA
87628820 5692806 Live/Registered
VANTA EDUCATION, INC.
2017-09-29
VANTA
VANTA
86749799 5080428 Live/Registered
Olympus Corporation
2015-09-08
VANTA
VANTA
86200796 4851899 Live/Registered
VANTA COMMERCIAL PROPERTIES L.L.C.
2014-02-21

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