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Timberline® Lateral Interbody Fusion System

FDA UDI

Class II (US FDA UDI)

by Biomet Spine Llc

Identity

Trade Name
Timberline® Lateral Interbody Fusion System FDA UDI
Generic Name
Polymeric spinal interbody fusion cage FDA UDI
Model / Reference
8725-5014 FDA UDI

Identifiers

Catalog Number
8725-5014 FDA UDI
Primary DI / UDI-DI
00887868209024 FDA UDI
FDA Product Code
MQP FDA UDI
MAX FDA UDI
GMDN Term
Polymeric spinal interbody fusion cage FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3060 FDA UDI
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

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Polymeric spinal interbody fusion cage

Timberline® Lateral Interbody Fusion System by Biomet Spine Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Polymeric spinal interbody fusion cage.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Biomet Spine Llc

Sources (1)

  • FDA UDI 2de977d6-ddf2-436b-bda5-e654951ac2be 35 fields · synced May 30, 2026