Vectris™ SureScan®

GUDID 00763000324292

LEAD 977A290 VECTRIS MRICS SUBCOMPACT

MEDTRONIC, INC.

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 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 ID00763000324292
NIH Device Record Keye37e51b3-86fb-412f-bf70-6bf8ea901df7
Commercial Distribution StatusIn Commercial Distribution
Brand NameVectris™ SureScan®
Version Model Number977A290
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

Device Dimensions

Length90 Centimeter
Length90 Centimeter
Length90 Centimeter
Length90 Centimeter
Length90 Centimeter
Length90 Centimeter
Length90 Centimeter
Length90 Centimeter
Length90 Centimeter
Length90 Centimeter
Length90 Centimeter
Length90 Centimeter
Length90 Centimeter
Length90 Centimeter
Length90 Centimeter
Length90 Centimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS100763000324292 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

QRBStimulator, spinal-cord, totally implanted for relief of pain due to diabetic neuropathy

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2022-03-07
Device Publish Date2022-02-26

On-Brand Devices [Vectris™ SureScan®]

00643169109421LEAD 977A160 MRICS SUBCOMPACT
00643169109414LEAD 977A175 MRICS SUBCOMPACT
00643169109407LEAD 977A190 MRICS SUBCOMPACT
00643169109391LEAD 977A260 MRICS COMPACT
00643169109384LEAD 977A275 MRICS COMPACT
00643169109377LEAD 977A290 MRICS COMPACT
00763000006549LEAD 977A290 VECTRIS MRICS SUBCOMPACT
00763000006525LEAD 977A275 VECTRIS MRICS SUBCOMPACT
00763000006501LEAD 977A260 VECTRIS MRICS SUBCOMPACT
00763000006488LEAD 977A190 VECTRIS MRICS SUBCOMPACT
00763000006464LEAD 977A175 VECTRIS MRICS SUBCOMPACT
00763000006440LEAD 977A160 VECTRIS MRICS SUBCOMPACT
00763000324292LEAD 977A290 VECTRIS MRICS SUBCOMPACT
00763000324285LEAD 977A275 VECTRIS MRICS SUBCOMPACT
00763000324278LEAD 977A260 VECTRIS MRICS SUBCOMPACT
00763000324261LEAD 977A190 VECTRIS MRICS SUBCOMPACT
00763000324254LEAD 977A175 VECTRIS MRICS SUBCOMPACT
00763000324247LEAD 977A160 VECTRIS MRICS SUBCOMPACT

Trademark Results [Vectris]

Mark Image

Registration | Serial
Company
Trademark
Application Date
VECTRIS
VECTRIS
85009043 4324744 Live/Registered
Medtronic, Inc.
2010-04-08
VECTRIS
VECTRIS
77185608 not registered Dead/Abandoned
Vectris Group Inc.
2007-05-21
VECTRIS
VECTRIS
75899678 not registered Dead/Abandoned
Pronto Aircraft, Corporation
2000-01-20
VECTRIS
VECTRIS
75878705 not registered Dead/Abandoned
Vectris Communications
1999-12-23
VECTRIS
VECTRIS
75175558 2166478 Dead/Cancelled
Ivoclar Vivadent, Inc.
1996-10-01

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