Veo Lateral Spinal System

GUDID 00840996177177

VEO Rasping Trail 17x9x6 deg

Choice Spine, LP

Polymeric spinal interbody fusion cage
Primary Device ID00840996177177
NIH Device Record Keye0db1df1-7cbd-4fcf-8c4a-cc913600f763
Commercial Distribution StatusIn Commercial Distribution
Brand NameVeo Lateral Spinal System
Version Model NumberV070-61709CG
Company DUNS078293017
Company NameChoice Spine, LP
Device Count1
DM Exempttrue
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(865)246-3333
Emailinfo@choicespine.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100840996177177 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

LXHORTHOPEDIC MANUAL SURGICAL INSTRUMENT

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00840996177177]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2020-02-24
Device Publish Date2019-06-20

On-Brand Devices [Veo Lateral Spinal System]

00840996177207VEO Rasping Trail 17x15x6 deg
00840996177191VEO Rasping Trail 17x13x6 deg
00840996177184VEO Rasping Trail 17x11x6 deg
00840996177177VEO Rasping Trail 17x9x6 deg
00840996177160VEO Rasping Trail 17x8x6 deg
00840996176422VEO, Ring Shavers
00840996176415VEO, Ring Shavers
00840996176408VEO, Ring Shavers

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