Battalion

FDA UDI

Class II (US FDA UDI)

by Alphatec Spine, Inc.

Identity

Trade Name: Battalion FDA UDI
Generic Name: Spinal implant trial FDA UDI
Device Name: Battalion PS Trial, SS, 9 mm wide, 5°, 25 mm X 15 mm FDA UDI
Model / Reference: 27002-106 FDA UDI
Description: Battalion PS Trial, SS, 9 mm wide, 5°, 25 mm X 15 mm FDA UDI

Identifiers

Primary DI / UDI-DI: 00844856008113 FDA UDI
510(k) Number: K143740 FDA UDI
FDA Product Code: MAX FDA UDI
GMDN Term: Spinal implant trial 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

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size: Angle — 5 degree FDA UDI
Height — 15 Millimeter FDA UDI
Width — 9 Millimeter FDA UDI
Length — 25 Millimeter FDA UDI

Category: Spinal implant trial

Battalion by Alphatec Spine, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Also classified as Spinal implant trial.

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TirboLOX-L Lumbar IBFD — Captiva Spine · Class II
Yellowstone — Summit Spine · Class II

Cleared under the same submission

K143740 also covers:

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: Alphatec Spine, Inc.

Sources (1)

FDA UDI 82a0a056-c4dd-465b-b16e-d492241f8163 36 fields · synced Jun 8, 2026