FDA.reportPublic FDA data

Lumbar IBFD

Primary DI
B084KPS22310140
Brand
Lumbar IBFD
Company
KEOS
Model
23L x 10W x 14H Straight, HA
Catalog number
KPS2-231014
Published
2018-02-22
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
Single use
true

Product Codes#

Code, Name table
CodeName
MAXIntervertebral Fusion Device With Bone Graft, Lumbar

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
MAXIntervertebral Fusion Device With Bone Graft, LumbarOrthopedic2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K160631000
K163386000
K193174000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K160631000Keos Lumbar IBFDKeos2016-07-15MAX
K163386000Keos Lumbar IBFDKeos2017-04-10MAX
K193174000Keos Lumbar IBFDKeos2019-12-16MAX

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
B084KPS22310140PrimaryHIBCC0

GMDN Terms#

Term, Definition table
TermDefinition
Polymeric 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 non-bioabsorbable synthetic polymer [e.g., polyetheretherketone (PEEK)] 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
Moist Heat or Steam Sterilization

Regulatory Flags#

DUNS number
080551837
Device count
1
Lot or batch
true
Manufacturing date on label
true
Sterilization required before use
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
B0842003800000Keos Lumbar InstrumentTamp, Straight200-38-00002023-02-10
B0842003800010Keos Lumbar InstrumentTamp, Straight, Bayoneted200-38-00012023-02-10
B0842004100100Keos Lumbar InstrumentGraft Pusher200-41-00102023-02-10
B084AC1141605070Anterior Cervical IBFD14D x 16W x 05H x 7L, PEEKAC1-141605-072024-02-09
B084AC1141606070Anterior Cervical IBFD14D x 16W x 06H x 7L, PEEKAC1-141606-072024-02-09
B084AC1141607070Anterior Cervical IBFD14D x 16W x 07H x 7L, PEEKAC1-141607-072024-02-09
B084AC1141608070Anterior Cervical IBFD14D x 16W x 08H x 7L, PEEKAC1-141608-072024-02-09
B084AC1141609070Anterior Cervical IBFD14D x 16W x 09H x 7L, PEEKAC1-141609-072024-02-09
B084AC1141610070Anterior Cervical IBFD14D x 16W x 10H x 7L, PEEKAC1-141610-072024-02-09
B084AC1141611070Anterior Cervical IBFD14D x 16W x 11H x 7L, PEEKAC1-141611-072024-02-09
B084AC1141612070Anterior Cervical IBFD14D x 16W x 12H x 7L, PEEKAC1-141612-072024-02-09
B084AC1161805000Anterior Cervical IBFD16D x 18W x 05H x 0L, PEEKAC1-161805-002024-02-09
B084AC1161805040Anterior Cervical IBFD16D x 18W x 05H x 4L, PEEKAC1-161805-042024-02-09
B084AC1161805070Anterior Cervical IBFD16D x 18W x 05H x 7L, PEEKAC1-161805-072024-02-09
B084AC1161806000Anterior Cervical IBFD16D x 18W x 06H x 0L, PEEKAC1-161806-002024-02-09
B084AC1161806040Anterior Cervical IBFD16D x 18W x 06H x 4L, PEEKAC1-161806-042024-02-09
B084AC1161806070Anterior Cervical IBFD16D x 18W x 06H x 7L, PEEKAC1-161806-072024-02-09
B084AC1161807000Anterior Cervical IBFD16D x 18W x 07H x 0L, PEEKAC1-161807-002024-02-09
B084AC1161807040Anterior Cervical IBFD16D x 18W x 07H x 4L, PEEKAC1-161807-042024-02-09
B084AC1161807070Anterior Cervical IBFD16D x 18W x 07H x 7L, PEEKAC1-161807-072024-02-09

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