Anterior Cervical Stabilization System (SSACSS), Kwik-Fix/TS® Cervical System

Primary DI
00815351020191
Brand
Anterior Cervical Stabilization System (SSACSS), Kwik-Fix/TS® Cervical System
Company
Southern Spine LLC
Model
1022T
Device description
Anterior Cervical Plate, Tissue Shield, 22mm
Published
2015-10-16
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

Related Records

Contact Domains

Product Codes

CodeName
KWQAPPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY

Product Code Classifications

CodeDeviceSpecialtyClass
KWQAppliance, Fixation, Spinal Intervertebral BodyOrthopedic2

Premarket Submissions

SubmissionSupplement
K063764000

Premarket Details

SubmissionSupplementDeviceApplicantDecision dateProduct code
K063764000SOUTHERN SPINE ANTERIOR CERVICAL STABILIZATION SYSTEM, KWIK- FIX CERVICAL SYSTEM, AND KWIK-FIX / TS CERVICAL SYSTEMSouthern Spine, LLC2007-05-16KWQ

Identifiers And Packaging

IdentifierTypeAgencyPackage quantityStatus
00815351020191PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifierGTIN-14 normalizedUPC-AEAN-13
00815351020191008153510201918153510201910815351020191

GMDN Terms

TermDefinition
Spinal fixation plate, non-bioabsorbableA small implantable sheet of solid material that is attached to the spine with screws for spinal immobilization and 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 typically used to provide immobilization and stabilization of spinal segments in the treatment of various spinal instabilities or deformities (e.g., during anterior/posterior cervical, anterior/posterior lumbar, thoracolumbar, and occipital fixation procedures).

Sterilization Methods

Method
Moist Heat or Steam Sterilization

Contacts

PhoneEmail
+1(478)330-6205donna@t3med.com

Regulatory Flags

DUNS number
794672225
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
false
Sterilization required before use
true

Other Devices From This Company

Primary DIBrandModelCatalogPublished
00815351022225Deploy™ Expandable Interbody SystemD-0008282022-01-10
00815351022232Deploy™ Expandable Interbody SystemD-0009282022-01-10
00815351022249Deploy™ Expandable Interbody SystemD-0010282022-01-10
00815351022256Deploy™ Expandable Interbody SystemD-0011282022-01-10
00815351022263Deploy™ Expandable Interbody SystemD-0012282022-01-10
00815351022270Deploy™ Expandable Interbody SystemD-0013282022-01-10
00815351022287Deploy™ Expandable Interbody SystemD-0014282022-01-10
00815351022294Deploy™ Expandable Interbody SystemD-0015282022-01-10
00815351022300Deploy™ Expandable Interbody SystemD-0016282022-01-10
00815351022317Deploy™ Expandable Interbody SystemD-0017282022-01-10
00815351022324Deploy™ Expandable Interbody SystemD-0008322022-01-10
00815351022331Deploy™ Expandable Interbody SystemD-0009322022-01-10
00815351022348Deploy™ Expandable Interbody SystemD-0010322022-01-10
00815351022478Deploy™ Expandable Interbody SystemD-0815282022-01-10
00815351022485Deploy™ Expandable Interbody SystemD-0816282022-01-10
00815351022492Deploy™ Expandable Interbody SystemD-0817282022-01-10
00815351022508Deploy™ Expandable Interbody SystemD-0810322022-01-10
00815351022515Deploy™ Expandable Interbody SystemD-0811322022-01-10
00815351022522Deploy™ Expandable Interbody SystemD-0812322022-01-10
00815351022539Deploy™ Expandable Interbody SystemD-0813322022-01-10

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08800071055440ASTEROSTEONIC CO.,Ltd.KWQ2026-03-19
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