BH113009D

GUDID 00841379181293

OTLIF SPACER, EXPANDABLE, NON-STERILE

HYHTE HOLDINGS, INC.

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Primary Device ID	00841379181293
NIH Device Record Key	e2742779-31b9-41f9-8b0d-f493115e6a23
Commercial Distribution Status	In Commercial Distribution
Version Model Number	BH113009D
Catalog Number	BH113009D
Company DUNS	073029645
Company Name	HYHTE HOLDINGS, INC.
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	false
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

Customer Support Contacts

Phone	7608148047
Email	TROY@ASTURAMEDICAL.COM
Phone	7608148047
Email	TROY@ASTURAMEDICAL.COM
Phone	7608148047
Email	TROY@ASTURAMEDICAL.COM
Phone	7608148047
Email	TROY@ASTURAMEDICAL.COM
Phone	7608148047
Email	TROY@ASTURAMEDICAL.COM
Phone	7608148047
Email	TROY@ASTURAMEDICAL.COM
Phone	7608148047
Email	TROY@ASTURAMEDICAL.COM

Device Dimensions

Length	30 Millimeter
Height	14 Millimeter
Angle	10 degree
Width	11 Millimeter
Length	30 Millimeter
Height	14 Millimeter
Angle	10 degree
Width	11 Millimeter
Length	30 Millimeter
Height	14 Millimeter
Angle	10 degree
Width	11 Millimeter
Length	30 Millimeter
Height	14 Millimeter
Angle	10 degree
Width	11 Millimeter
Length	30 Millimeter
Height	14 Millimeter
Angle	10 degree
Width	11 Millimeter
Length	30 Millimeter
Height	14 Millimeter
Angle	10 degree
Width	11 Millimeter
Length	30 Millimeter
Height	14 Millimeter
Angle	10 degree
Width	11 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	00841379181293 [Primary]

FDA Product Code

MAX	Intervertebral Fusion Device With Bone Graft, Lumbar