ASTRA-OCT Spine System

Primary DI
00193082083204
Brand
ASTRA-OCT Spine System
Company
SPINECRAFT, LLC
Model
A3S-XN
Catalog number
A3S-XN
Device description
ASTRA-OCT Cross Connector Nut
Published
2018-10-03
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
OTC
false
Sterile
false
Single use
true

Contact Domains#

Product Codes#

Code, Name table
CodeName
NKGOrthosis, cervical pedicle screw spinal fixation

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
NKGPosterior Cervical Screw SystemOrthopedic2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K181350000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K181350000ASTRA-OCT Spine SystemSpinecraft, LLC2018-07-06NKG

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
M824A3SXN1PrimaryHIBCC0
00193082083204SecondaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00193082083204001930820832041930820832040193082083204

GMDN Terms#

Term, Definition table
TermDefinition
Spinal bone set screwA small, threaded, implantable, non-bioabsorbable disc intended to be threaded into the proximal end of a spinal bone screw (screw head), anchor, connector and/or hook (none included) to secure/stabilize a rod and/or tether as part of an internal spinal fixation procedure or a treatment for idiopathic scoliosis. It is made of metal (e.g., surgical steel, titanium alloy).

Sterilization Methods#

Method table
Method
Moist Heat or Steam Sterilization

Contacts#

Phone, Email table
PhoneEmail
+1(999)999-1112info@device.com

Regulatory Flags#

DUNS number
783908713
Device count
1
DM exempt
false
Premarket exempt
false
HCT/P
false
Kit
false
Combination product
false
Lot or batch
true
Serial number
false
Manufacturing date on label
false
Expiration date on label
false
Donation ID number
false
Contains natural rubber latex
false
No natural rubber latex
true
Sterilization required before use
true

Other Devices From This Company#

Primary DI, Brand, Model table
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00193082162107ANTERIS Thoracolumbar Plate SystemLPS-APSD-14LPS-APSD-142026-05-20
00193082162114ANTERIS Thoracolumbar Plate SystemLPS-APSD-16LPS-APSD-162026-05-20
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00193082162152ANTERIS Thoracolumbar Plate SystemLPS-APSD-24LPS-APSD-242026-05-20
00193082162169ANTERIS Thoracolumbar Plate SystemLPS-APSL-10LPS-APSL-102026-05-20
00193082162176ANTERIS Thoracolumbar Plate SystemLPS-APSL-12LPS-APSL-122026-05-20
00193082162183ANTERIS Thoracolumbar Plate SystemLPS-APSL-14LPS-APSL-142026-05-20
00193082162190ANTERIS Thoracolumbar Plate SystemLPS-APSL-16LPS-APSL-162026-05-20
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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