ASTRA Spine System

Primary DI
M824A5U55401
Brand
ASTRA Spine System
Company
SPINECRAFT, LLC
Model
A5U-5540
Device description
ASTRA Ti Uniplanar Screw 5.50 x 40mm
Published
2015-09-11
Public version status
Update
Distribution status
Not in Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
Single use
true

Contact Domains#

Product Codes#

Code, Name table
CodeName
KWPAPPLIANCE, FIXATION, SPINAL INTERLAMINAL
KWQAPPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY
MNHOrthosis, spondylolisthesis spinal fixation
MNIORTHOSIS, SPINAL PEDICLE FIXATION
NKBOrthosis, spinal pedicle fixation, for degenerative disc disease

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
KWPAppliance, Fixation, Spinal InterlaminalOrthopedic2
KWQAppliance, Fixation, Spinal Intervertebral BodyOrthopedic2
MNHOrthosis, Spondylolisthesis Spinal FixationOrthopedic2
MNIOrthosis, Spinal Pedicle FixationOrthopedic2
NKBThoracolumbosacral Pedicle Screw SystemOrthopedic2

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
M824A5U55401PrimaryHIBCC0

GMDN Terms#

Term, Definition table
TermDefinition
Spinal bone screw, non-bioabsorbableA small, threaded, implantable rod with a slotted head intended to be used for internal spinal fixation by being screwed into the spine to hold a correction/stabilization device (e.g., rod, plate, tether) to bone; it is made of a material that is not chemically degraded or absorbed via natural body processes (includes implant grade metal such as surgical steel, titanium alloy, or carbon fibre). The device is available in various types, including pedicle and transfacet, and is typically used to provide immobilization and stabilization of spinal segments in the treatment of various spinal instabilities or deformities.

Sterilization Methods#

Method table
Method
Moist Heat or Steam Sterilization

Contacts#

Phone, Email table
PhoneEmail
+1(630)920-7300info@spinecraft.com

Regulatory Flags#

DUNS number
783908713
Device count
1
Lot or batch
true
No natural rubber latex
true
Sterilization required before use
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
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00193082162206ANTERIS Thoracolumbar Plate SystemLPS-APSL-18LPS-APSL-182026-05-20
00193082162213ANTERIS Thoracolumbar Plate SystemLPS-APSL-20LPS-APSL-202026-05-20
00193082162220ANTERIS Thoracolumbar Plate SystemLPS-APSL-22LPS-APSL-222026-05-20
00193082162237ANTERIS Thoracolumbar Plate SystemLPS-APSL-24LPS-APSL-242026-05-20
00193082162688ANTERIS Thoracolumbar Plate SystemLPS-APS50-30LPS-APS50-302026-05-20
00193082162695ANTERIS Thoracolumbar Plate SystemLPS-APS55-30LPS-APS55-302026-05-20
00193082162701ANTERIS Thoracolumbar Plate SystemLPS-APS50-20LPS-APS50-202026-05-20
00193082162718ANTERIS Thoracolumbar Plate SystemLPS-APS55-20LPS-APS55-202026-05-20

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