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Vail ALIF Buttress Plate System

FDA UDI

Class II (US FDA UDI)

by Evolution Spine, Llc

Identity

Trade Name
Vail ALIF Buttress Plate System FDA UDI
Generic Name
Spinal fixation plate, non-bioabsorbable FDA UDI
Device Name
24mm 6 Deg Buttress Plate FDA UDI
Model / Reference
BP132406 FDA UDI
Description
24mm 6 Deg Buttress Plate FDA UDI

Identifiers

Catalog Number
BP132406 FDA UDI
Primary DI / UDI-DI
00195860010631 FDA UDI
510(k) Number
K180755 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

Dimensions & Sizes

Size
Length — 24 Millimeter FDA UDI
Angle — 6 degree FDA UDI

Category: Spinal fixation plate, non-bioabsorbable

Vail ALIF Buttress Plate System by Evolution Spine, Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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

Sources (1)

  • FDA UDI b2ee13c2-a47f-40b1-a190-572ae33c3831 37 fields · synced May 31, 2026