Omnia Medical TiBrid™-A

GUDID 00843511110475

TiBrid™-A RASP, 36x27x12mm, 20°

OMNIA MEDICAL, LLC

Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable

Primary Device ID	00843511110475
NIH Device Record Key	cb4d095d-f007-4765-90c2-5088c2c55ec9
Commercial Distribution Status	In Commercial Distribution
Brand Name	Omnia Medical TiBrid™-A
Version Model Number	14-5A-RA362712-20
Company DUNS	079467378
Company Name	OMNIA MEDICAL, 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	false
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	3044134851
Email	customerservice@omniamedical.com
Phone	3044134851
Email	customerservice@omniamedical.com
Phone	3044134851
Email	customerservice@omniamedical.com
Phone	3044134851
Email	customerservice@omniamedical.com
Phone	3044134851
Email	customerservice@omniamedical.com
Phone	3044134851
Email	customerservice@omniamedical.com
Phone	3044134851
Email	customerservice@omniamedical.com
Phone	3044134851
Email	customerservice@omniamedical.com
Phone	3044134851
Email	customerservice@omniamedical.com
Phone	3044134851
Email	customerservice@omniamedical.com
Phone	3044134851
Email	customerservice@omniamedical.com
Phone	3044134851
Email	customerservice@omniamedical.com
Phone	3044134851
Email	customerservice@omniamedical.com
Phone	3044134851
Email	customerservice@omniamedical.com
Phone	3044134851
Email	customerservice@omniamedical.com
Phone	3044134851
Email	customerservice@omniamedical.com
Phone	3044134851
Email	customerservice@omniamedical.com

Device Dimensions

Width	36 Millimeter
Length	27 Millimeter
Height	12 Millimeter
Angle	20 degree
Width	36 Millimeter
Length	27 Millimeter
Height	12 Millimeter
Angle	20 degree
Width	36 Millimeter
Length	27 Millimeter
Height	12 Millimeter
Angle	20 degree
Width	36 Millimeter
Length	27 Millimeter
Height	12 Millimeter
Angle	20 degree
Width	36 Millimeter
Length	27 Millimeter
Height	12 Millimeter
Angle	20 degree
Width	36 Millimeter
Length	27 Millimeter
Height	12 Millimeter
Angle	20 degree
Width	36 Millimeter
Length	27 Millimeter
Height	12 Millimeter
Angle	20 degree
Width	36 Millimeter
Length	27 Millimeter
Height	12 Millimeter
Angle	20 degree
Width	36 Millimeter
Length	27 Millimeter
Height	12 Millimeter
Angle	20 degree
Width	36 Millimeter
Length	27 Millimeter
Height	12 Millimeter
Angle	20 degree
Width	36 Millimeter
Length	27 Millimeter
Height	12 Millimeter
Angle	20 degree
Width	36 Millimeter
Length	27 Millimeter
Height	12 Millimeter
Angle	20 degree
Width	36 Millimeter
Length	27 Millimeter
Height	12 Millimeter
Angle	20 degree
Width	36 Millimeter
Length	27 Millimeter
Height	12 Millimeter
Angle	20 degree
Width	36 Millimeter
Length	27 Millimeter
Height	12 Millimeter
Angle	20 degree
Width	36 Millimeter
Length	27 Millimeter
Height	12 Millimeter
Angle	20 degree
Width	36 Millimeter
Length	27 Millimeter
Height	12 Millimeter
Angle	20 degree

Device Identifiers

Device Issuing Agency	Device ID
GS1	00843511110475 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

Premarket Notification: K190363

FDA Product Code

MAX	Intervertebral Fusion Device With Bone Graft, Lumbar