FDA.reportPublic FDA data

Biolign

Primary DI
06009696227900
Brand
Biolign
Company
ELITE SURGICAL SUPPLIES (PTY) LTD
Model
BCC150406
Catalog number
BCC150406
Device description
Cervical Cage 15 x 4 x 6mm
Published
2016-09-24
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
MR Conditional
Rx
true
Sterile
true
Single use
true

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

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K130274000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K130274000BIOLIGN ACIF SYSTEMS, BIOLIGN STACC ACIF SYSTEM, BIOLIGN TLIF SYSTEMElite Surgical Supplies (Pty), Ltd.2013-10-29MAX

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
06009696227900PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, EAN-13 table
Source identifierGTIN-14 normalizedEAN-13
06009696227900060096962279006009696227900

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.

Sterilization Methods#

Method table
Method

Regulatory Flags#

DUNS number
568359710
Device count
1
Lot or batch
true
Manufacturing date on label
true
Expiration date on label
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
06009696221076VertefixSP5535TSP5535T2016-09-22
06009696221083VertefixSP5540TSP5540T2016-09-23
06009696221090VertefixSP5545TSP5545T2016-09-23
06009696221106VertefixSP5550TSP5550T2016-09-23
06009696221120VertefixSP6535TSP6535T2016-09-23
06009696221137VertefixSP6540TSP6540T2016-09-23
06009696221144VertefixSP6545TSP6545T2016-09-23
06009696221151VertefixSP6550TSP6550T2016-09-23
06009696221175VertefixSP7535TSP7535T2016-09-23
06009696221182VertefixSP7540TSP7540T2016-09-23
06009696221199VertefixSP7545TSP7545T2016-09-23
06009696221205VertefixSP7550TSP7550T2016-09-23
06009696221229VertefixMA5535TMA5535T2016-09-23
06009696221236VertefixMA5540TMA5540T2016-09-23
06009696221243VertefixMA5545TMA5545T2016-09-23
06009696221250VertefixMA5550TMA5550T2016-09-23
06009696221274VertefixMA6535TMA6535T2016-09-23
06009696221281VertefixMA6540TMA6540T2016-09-23
06009696221298VertefixMA6545TMA6545T2016-09-23
06009696221304VertefixMA6550TMA6550T2016-09-23

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Primary DI, Brand, Company table
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18257200031382CONSTRUX - MINI PTCOrthofix US LLCODP2026-07-17