AVS Anchor-C Cervical Cage System 48328708

GUDID 07613327267310

TRIAL

Stryker Corporation

Spinal implant trial
Primary Device ID07613327267310
NIH Device Record Key63feb959-6956-4025-96a5-f8fa082c7dd4
Commercial Distribution StatusIn Commercial Distribution
Brand NameAVS Anchor-C Cervical Cage System
Version Model Number48328708
Catalog Number48328708
Company DUNS149183167
Company NameStryker Corporation
Device Count1
DM Exemptfalse
Pre-market Exempttrue
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 Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Dimensions

Depth12 Millimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS107613327267310 [Primary]

FDA Product Code

LXHORTHOPEDIC MANUAL SURGICAL INSTRUMENT

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[07613327267310]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2019-12-10
Device Publish Date2019-12-02

On-Brand Devices [AVS Anchor-C Cervical Cage System]

07613327267662DRILL BIT
07613327267631DRILL BIT
07613327267549DRILL BIT
07613327126280FLEXIBLE DRILL
07613327010213FLEXIBLE DRILL
07613327010206FLEXIBLE DRILL
07613327119459IMPLANT CADDY
07613327119442SCREW CADDY
07613327119435CONTAINER
07613327267587TRIAL
07613327267556TRIAL
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07613327267396TRIAL
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07613327267310TRIAL
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07613327267136TRIAL

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