FDA.reportPublic FDA data

Keos Lumbar Instrument

Primary DI
B0842004200020
Brand
Keos Lumbar Instrument
Company
KEOS
Model
Nerve Root Suction Retractor, w/ Lip, 210mm
Catalog number
200-42-0002
Published
2023-02-10
Public version status
New
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true

Product Codes#

Code, Name table
CodeName
LXHOrthopedic Manual Surgical Instrument

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
LXHOrthopedic Manual Surgical InstrumentOrthopedic1

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
B0842004200020PrimaryHIBCC0

GMDN Terms#

Term, Definition table
TermDefinition
Nerve/vessel retractorA hand-held, non-self-retaining surgical instrument intended to be used for retracting a nerve, tendon, or blood vessel to separate it from the surrounding tissue primarily to allow access to other tissues during a surgical intervention. It is a shaft-like metallic instrument with a blunt bulbous or rounded hook-like retraction tip at the distal end, and a handle at the proximal end. It is available in a variety of designs such as, curved, right-angled, or 45 degree angled. This is a reusable device.

Sterilization Methods#

Method table
Method
Moist Heat or Steam Sterilization

Regulatory Flags#

DUNS number
080551837
Device count
1
Premarket exempt
true
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
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B084AC1141607070Anterior Cervical IBFD14D x 16W x 07H x 7L, PEEKAC1-141607-072024-02-09
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