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ATEC Lateral Navigation Disc Prep Instruments

FDA UDI

Class II (US FDA UDI)

by Alphatec Spine, Inc.

Identity

Trade Name
ATEC Lateral Navigation Disc Prep Instruments FDA UDI
Generic Name
Orthopaedic osteotome FDA UDI
Device Name
LIF NAV OSTEOTOME 12mm FDA UDI
Model / Reference
266-01-000-12-N FDA UDI
Description
LIF NAV OSTEOTOME 12mm FDA UDI

Identifiers

Primary DI / UDI-DI
00190376476186 FDA UDI
510(k) Number
K223765 FDA UDI
FDA Product Code
OLO FDA UDI
GMDN Term
Orthopaedic osteotome FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.4560 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

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size
Width — 12 Millimeter FDA UDI

Category: Orthopaedic osteotome

ATEC Lateral Navigation Disc Prep Instruments by Alphatec Spine, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic osteotome.

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 18dbd257-6498-4e87-8320-915da379bef2 36 fields · synced Jun 8, 2026