NuVasive

GUDID 00887517391308

CoRoent XLW Trial, 8x22x60mm 10°

Nuvasive, Inc.

Spinal implant trial Spinal implant trial
Primary Device ID00887517391308
NIH Device Record Key999787c9-06ea-4120-afe2-3cc749c9c38e
Commercial Distribution StatusIn Commercial Distribution
Brand NameNuVasive
Version Model Number6910608
Company DUNS053950783
Company NameNuvasive, Inc.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numberfalse
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(858)909-1800
EmailRA_UDI@nuvasive.com
Phone+1(858)909-1800
EmailRA_UDI@nuvasive.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100887517391308 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

PHMIntervertebral fusion device with bone graft, thoracic

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00887517391308]

Moist Heat or Steam Sterilization


[00887517391308]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2019-02-07
Device Publish Date2018-09-17

On-Brand Devices [NuVasive]

00887517533982Universal Threaded Pin, Bone Mill
00887517498182Universal Counter Torque
00887517488671Universal Guide, Size 10 Bone Mill
00887517488657Universal Guide, Size 6 Bone Mill
00887517451552Universal Graft Pusher, Cervical Solid
00887517429209Univ Pedicle Probe, Ball Tip Curved
00887517428998Universal Probe, Ball-Tip
00887517405449CoRoent XLR Driver, Detachable
00887517391339CoRoent XLW Trial, 14x22x60mm 10°
00887517391322CoRoent XLW Trial, 12x22x60mm 10°
00887517391315CoRoent XLW Trial, 10x22x60mm 10°
00887517391308CoRoent XLW Trial, 8x22x60mm 10°
00887517390974CoRoent XLW Trial, 12x22x50mm 10°
00887517390967CoRoent XLW Trial, 10x22x50mm 10°
00887517390950CoRoent XLW Trial, 8x22x50mm 10°
00887517389091Universal Inserter, XLIF Angled
00887517389084Universal Tamp, XLIF Angled
00887517389077Universal Rasp, Angled
00887517389053Universal Currette, Angled Down Medium
00887517389046Universal Currette, Angled Up Medium
00887517389039Universal Cobb, Down Large
00887517389022Universal Cobb, Up Large
00887517389015Universal Cobb, Angled Down Small
00887517389008Universal Cobb, Angled Up Small
00887517388698Universal Rongeur, Angled Left Large
00887517388681Universal Rongeur, Angled Right Large
00887517388674Universal Rongeur, Med Angled Left
00887517388667Universal Rongeur, Med Angled Right
00887517388650Universal Broach 10x18mm Angled
00887517388643Universal Broach 8x18mm Angled
00887517388636Universal Broach 6x18mm Angled
00887517388209Universal Trial 12x22x60mm CoRoent XLW
00887517387899Universal Trial 10x22x60mm CoRoent XLW
00887517387882Universal Trial 8x22x60mm CoRoent XLW
00887517387851Universal Trial 12x22x50mm CoRoent XLW
00887517387844Universal Trial 10x22x50mm CoRoent XLW
00887517387837Universal Trial 8x22x50mm CoRoent XLW
00887517386595Universal Guide, Drill
00887517386557Universal Drill, 2.5mm Extractor
00887517386533Universal Extractor, 4.5mm Tap
00887517386526Universal Extractor, 3.5mm Tap
00887517386519Universal Extractor, 2.5mm Tap
00887517385840Universal Osteotome, 16 Straight
00887517385802Universal Rongeur, Pituitary Small
00887517385536Universal Rasp, Serrated Thoracic
00887517383068Universal Disc Cutter, 6mm AL
00887517383020Universal Rongeur, 2mm Kerrison
00887517382351Universal Inserter, CoRoent XL
00887517381910Universal Curette, 2mm Down Facing
00887517381903Universal Curette, X-Small Up Angled

Trademark Results [NuVasive]

Mark Image

Registration | Serial
Company
Trademark
Application Date
NUVASIVE
NUVASIVE
76298757 2818737 Live/Registered
NUVASIVE, INC.
2001-08-10
NUVASIVE
NUVASIVE
75822001 2541247 Live/Registered
NUVASIVE, INC.
1999-10-13

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