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Brickyard Stand-Alone ALIF

FDA UDI

Class II (US FDA UDI)

by Altus Spine

Identity

Trade Name
Brickyard Stand-Alone ALIF FDA UDI
Generic Name
Spinal bone screw, non-bioabsorbable FDA UDI
Device Name
Titanium Screw, 4.2mmx30mm FDA UDI
Model / Reference
SLV4230 FDA UDI
Description
Titanium Screw, 4.2mmx30mm FDA UDI

Identifiers

Primary DI / UDI-DI
00843210180052 FDA UDI
510(k) Number
K211837 FDA UDI
FDA Product Code
MAX FDA UDI
GMDN Term
Spinal bone screw, non-bioabsorbable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3080 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

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Spinal bone screw, non-bioabsorbable

Brickyard Stand-Alone ALIF by Altus Spine — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Spinal bone screw, 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
Altus Spine

Sources (1)

  • FDA UDI 977076a8-3a87-4fcf-8f2f-27909904d2d0 35 fields · synced Jun 1, 2026