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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
Bone tap, reprocessed FDA UDI
Device Name
45° Geared Ø4.2mm Tap Tip, 15mm FDA UDI
Model / Reference
1030-4215G-45 FDA UDI
Description
45° Geared Ø4.2mm Tap Tip, 15mm FDA UDI

Identifiers

Primary DI / UDI-DI
00843210186689 FDA UDI
510(k) Number
K211837 FDA UDI
FDA Product Code
MAX FDA UDI
OVD FDA UDI
GMDN Term
Bone tap, reprocessed 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

No

FDA UDI

Implantable

No

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: Bone tap, reprocessed

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

Similar devices

Also classified as Bone tap, reprocessed.

Cleared under the same submission

K211837 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Altus Spine

Sources (1)

  • FDA UDI 769bf89f-778f-4574-889f-c5640196b466 35 fields · synced May 30, 2026