Kingsnake

GUDID B014KS3110

EMINENT SPINE LLC

Polymeric spinal interbody fusion cage
Primary Device IDB014KS3110
NIH Device Record Key7cb71ad8-4651-404e-95d5-0a4c9577a39e
Commercial Distribution StatusIn Commercial Distribution
Brand NameKingsnake
Version Model NumberKS3110
Company DUNS022576742
Company NameEMINENT 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 Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
HIBCCB014KS3110 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

MQPSpinal Vertebral Body Replacement Device

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[B014KS3110]

Moist Heat or Steam Sterilization


[B014KS3110]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2020-02-24
Device Publish Date2017-02-09

On-Brand Devices [Kingsnake]

B014KS7113KS7113
B014KS7112KS7112
B014KS7111KS7111
B014KS7110KS7110
B014KS7109KS7109
B014KS7108KS7108
B014KS7013KS7013
B014KS7012KS7012
B014KS7011KS7011
B014KS7010KS7010
B014KS7009KS7009
B014KS7008KS7008
B014KS5113KS5113
B014KS5112KS5112
B014KS5111KS5111
B014KS5110KS5110
B014KS5109KS5109
B014KS5108KS5108
B014KS5013KS5013
B014KS5012KS5012
B014KS5011KS5011
B014KS5010KS5010
B014KS5009KS5009
B014KS5008KS5008
B014KS3113KS3113
B014KS3112KS3112
B014KS3111KS3111
B014KS3110KS3110
B014KS3109KS3109
B014KS3108KS3108
B014KS3013KS3013
B014KS3012KS3012
B014KS3011KS3011
B014KS3010KS3010
B014KS3009KS3009
B014KS3008KS3008
B014KS3007KS3007

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