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

FDA UDI

Class II (US FDA UDI)

by Southern Spine LLC

Identity

Trade Name
Anterior Cervical Stabilization System (SSACSS), Kwik-Fix® Cervical System FDA UDI
Generic Name
Spinal fixation plate, non-bioabsorbable FDA UDI
Device Name
Anterior Cervical Plate, 66mm FDA UDI
Model / Reference
3066 FDA UDI
Description
Anterior Cervical Plate, 66mm FDA UDI

Identifiers

Primary DI / UDI-DI
00815351020139 FDA UDI
510(k) Number
K021979 FDA UDI
FDA Product Code
KWQ FDA UDI
GMDN Term
Spinal fixation plate, non-bioabsorbable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3060 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Spinal fixation plate, non-bioabsorbable

Anterior Cervical Stabilization System (SSACSS), Kwik-Fix® Cervical System by Southern Spine LLC — Class II — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Spinal fixation plate, non-bioabsorbable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Southern Spine LLC

Sources (1)

  • FDA UDI 5cac88af-2b57-4c6e-add6-84a5032ffd81 35 fields · synced May 30, 2026