DOC 73100170

GUDID 10705034014661

DOC VENTRAL CERVICAL STABILIZATION SYSTEM FINLESS NONLOCKING PLATFORM

DEPUY SPINE, LLC

Bone-screw internal spinal fixation system, non-sterile
Primary Device ID10705034014661
NIH Device Record Key8893efc3-8989-48cb-bae4-3d32f3222945
Commercial Distribution Discontinuation2019-11-30
Commercial Distribution StatusIn Commercial Distribution
Brand NameDOC
Version Model Number73100170
Catalog Number73100170
Company DUNS107105876
Company NameDEPUY SPINE, LLC
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 Usetrue
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(800)255-2500
Emailxx@xx.xx

Device Identifiers

Device Issuing AgencyDevice ID
GS110705034014661 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

KWQAPPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[10705034014661]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2019-11-07
Device Publish Date2015-09-24

On-Brand Devices [DOC]

10705034014678DOC VENTRAL CERVICAL STABILIZATION SYSTEM FINLESS LOCKING PLATFORM
10705034014661DOC VENTRAL CERVICAL STABILIZATION SYSTEM FINLESS NONLOCKING PLATFORM
10705034014654DOC VENTRAL CERVICAL STABILIZATION SYSTEM DIVERGENT PLATFORM LOCKING
10705034014647DOC VENTRAL CERVICAL STABILIZATION SYSTEM DIVERGENT PLATFORM NONLOCKING

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