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: Surgical screwdriver, reusable FDA UDI
Device Name: 45° Geared Ø4.2mm Drill Tip, 35mm FDA UDI
Model / Reference: 1030-0235G-45 FDA UDI
Description: 45° Geared Ø4.2mm Drill Tip, 35mm FDA UDI

Identifiers

Primary DI / UDI-DI: 00843210180519 FDA UDI
510(k) Number: K211837 FDA UDI
FDA Product Code: MAX FDA UDI
OVD FDA UDI
GMDN Term: Surgical screwdriver, reusable 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

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Surgical screwdriver, reusable

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

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Also classified as Surgical screwdriver, reusable.

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USS — Synthes · Class I
Whistler Modular Pedicle Screw System — EVOLUTION SPINE, LLC · Class I
CosmoLock Pedicle Screw System — Kalitec Direct LLC · Class I

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Altus Spine

Sources (1)

FDA UDI 76032b59-f1a2-47b7-b34a-6607cd4507d6 35 fields · synced Jun 8, 2026