FDA.reportPublic FDA data

Ti-Largo™

Primary DI
B18300911147130
Brand
Ti-Largo™
Company
FLOSPINE LLC
Model
Ti-Largo™
Catalog number
09-1114-713
Device description
Cervical Interbody, 11mm x 14mm x 13mm, 7°
Published
2023-08-25
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
Sterile
true
Single use
true

Contact Domains#

Product Codes#

Code, Name table
CodeName
ODPIntervertebral Fusion Device With Bone Graft, Cervical

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
ODPIntervertebral Fusion Device With Bone Graft, CervicalOrthopedic2

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
B18300911147130PrimaryHIBCC0

GMDN Terms#

Term, Definition table
TermDefinition
Metallic spinal interbody fusion cageA device intended to be implanted into the space of an intervertebral disc that has been partially or totally removed during surgery in order to allow bone fusion between two contiguous vertebral bodies, typically in the treatment of degenerative disc disease (DDD). It is in the form of a hollow, porous, threaded and/or fenestrated cylindrical or geometrical device made of metal [e.g., titanium (Ti)] that provides mechanical stability and sufficient space for therapeutic spinal bone fusion to occur; bone graft is typically used to help with osseointegration. Fixation screws and devices associated with implantation may be included with the device.

Device Sizes#

Type, Value, Unit table
TypeValueUnit
Angle7degree
Height13Millimeter
Length11Millimeter
Width14Millimeter

Sterilization Methods#

Method table
Method

Contacts#

Phone, Email table
PhoneEmail
(561)705-3080info@flospine.com

Regulatory Flags#

DUNS number
042993143
Device count
1
Lot or batch
true
Expiration date on label
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
B1830802450120Panama™Panama™08-0245-0122021-09-01
B1830802450140Panama™Panama™08-0245-0142021-09-01
B1830802450160Panama™Panama™08-0245-0162021-09-01
B1830802450180Panama™Panama™08-0245-0182021-09-01
B1830802450200Panama™Panama™08-0245-0202021-09-01
B1830803400120Panama™Panama™08-0340-0122021-09-01
B1830803400140Panama™Panama™08-0340-0142021-09-01
B1830803400160Panama™Panama™08-0340-0162021-09-01
B1830803400180Panama™Panama™08-0340-0182021-09-01
B1830803400200Panama™Panama™08-0340-0202021-09-01
B1830803450120Panama™Panama™08-0345-0122021-09-01
B1830803450140Panama™Panama™08-0345-0142021-09-01
B1830803450160Panama™Panama™08-0345-0162021-09-01
B1830803450180Panama™Panama™08-0345-0182021-09-01
B1830803450200Panama™Panama™08-0345-0202021-09-01
B1830804400120Panama™Panama™08-0440-0122021-09-01
B1830804400140Panama™Panama™08-0440-0142021-09-01
B1830804400160Panama™Panama™08-0440-0162021-09-01
B1830804400180Panama™Panama™08-0440-0182021-09-01
B1830804400200Panama™Panama™08-0440-0202021-09-01

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Primary DI, Brand, Company table
Primary DIBrandCompanyProduct codePublished
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00810017915149SABER-XA, Screw Ø5.0 x 32.5ELEVATION SPINE, INC.ODP2026-09-22
00810017915156SABER-XA, Screw Ø5.5 x 22.5ELEVATION SPINE, INC.ODP2026-09-22
00810017915163SABER-XA, Screw Ø5.5 x 27.5ELEVATION SPINE, INC.ODP2026-09-22
07613327503968Aero-CStryker CorporationODP2019-12-18
10888857461819CASCADIA™ Interbody SystemVB Spine LLCODP2019-10-31
10888857461888CASCADIA™ Interbody SystemVB Spine LLCODP2019-10-31
07613327353921Aero-CStryker CorporationODP2018-06-28
07613327353938Aero-CStryker CorporationODP2018-06-28
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07613327360516Tritanium CStryker CorporationODP2017-09-18
07613252602774AVS Anchor-LStryker CorporationODP2016-09-24