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

Primary DI
00815351021907
Brand
Anterior Cervical Stabilization System (SSACSS), Kwik-Fix/TS® Cervical System
Company
Southern Spine LLC
Model
38100
Device description
Universal Handle
Published
2016-08-04
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
false

Contact Domains#

Product Codes#

Code, Name table
CodeName
KWQAPPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
KWQAppliance, Fixation, Spinal Intervertebral BodyOrthopedic2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K021979000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K021979000SMISSON STABILIZATION SYSTEMSmisson-Cartledge2003-06-27KWQ

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00815351021907PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00815351021907008153510219078153510219070815351021907

GMDN Terms#

Term, Definition table
TermDefinition
Surgical instrument handle, non-torque-limitingA hand-held manual surgical instrument designed to attach to the proximal end of a surgical instrument (e.g., a screwdriver shaft) to allow the surgeon to perform manipulations with the instrument, such as manual rotation of a bone screw or reamer; it does not include a torque-limiting function. The device is typically made of metal and/or synthetic material and may have a straight or T-shaped handle grip which may include additional features such as a ratchet mechanism to allow the surgeon to maintain a constant hold on the handle when providing rotation in one direction. This is a reusable device.

Sterilization Methods#

Method table
Method
Moist Heat or Steam Sterilization

Contacts#

Phone, Email table
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 DI, Brand, Model table
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

Other Devices Sharing Product Codes#

Primary DI, Brand, Company table
Primary DIBrandCompanyProduct codePublished
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00763000663360ZEVO™ Anterior Cervical Plate SystemMEDTRONIC SOFAMOR DANEK, INC.KWQ2026-03-19
00840283402197VyPlate™VY SPINE LLCKWQ2026-03-19
00840283402203VyPlate™VY SPINE LLCKWQ2026-03-19
08800071055440ASTEROSTEONIC CO.,Ltd.KWQ2026-03-19
00763000889982VENTURE™ Anterior Cervical Plate SystemMEDTRONIC SOFAMOR DANEK, INC.KWQ2026-03-16
00763000889999VENTURE™ Anterior Cervical Plate SystemMEDTRONIC SOFAMOR DANEK, INC.KWQ2026-03-16
00763000890001VENTURE™ Anterior Cervical Plate SystemMEDTRONIC SOFAMOR DANEK, INC.KWQ2026-03-16
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00763000890094VENTURE™ Anterior Cervical Plate SystemMEDTRONIC SOFAMOR DANEK, INC.KWQ2026-03-16
00763000890100VENTURE™ Anterior Cervical Plate SystemMEDTRONIC SOFAMOR DANEK, INC.KWQ2026-03-16
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00763000890124VENTURE™ Anterior Cervical Plate SystemMEDTRONIC SOFAMOR DANEK, INC.KWQ2026-03-16
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00763000890186VENTURE™ Anterior Cervical Plate SystemMEDTRONIC SOFAMOR DANEK, INC.KWQ2026-03-16
00763000890193VENTURE™ Anterior Cervical Plate SystemMEDTRONIC SOFAMOR DANEK, INC.KWQ2026-03-16
00763000890209VENTURE™ Anterior Cervical Plate SystemMEDTRONIC SOFAMOR DANEK, INC.KWQ2026-03-16
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