Kingsnake

GUDID B014KS5110

Polymeric spinal interbody fusion cage

Primary Device ID	B014KS5110
NIH Device Record Key	aa59a171-44f5-44b6-bb40-78f6443e1307
Commercial Distribution Status	In Commercial Distribution
Brand Name	Kingsnake
Version Model Number	KS5110
Company DUNS	022576742
Company Name	EMINENT SPINE LLC
Device Count	1
DM Exempt	false
Pre-market Exempt	false
MRI Safety Status	Labeling does not contain MRI Safety Information
Human Cell/Tissue Product	false
Device Kit	false
Device Combination Product	false
Single Use	true
Lot Batch	true
Serial Number	false
Manufacturing Date	true
Expiration Date	false
Donation Id Number	false
Contains Natural Rubber Latex	false
Labeled No Natural Rubber Latex	false
RX Perscription	true
OTC Over-The-Counter	false

Device Issuing Agency	Device ID
HIBCC	B014KS5110 [Primary]

MQP	Spinal Vertebral Body Replacement Device

Steralize Prior To Use	true
Device Is Sterile	false

[B014KS5110]

Moist Heat or Steam Sterilization

[B014KS5110]

Moist Heat or Steam Sterilization