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Timberline Mpf Lateral Modular Plate Fixation System

FDA UDI

Class II (US FDA UDI)

by Biomet Spine Llc

Identity

Trade Name
TIMBERLINE MPF LATERAL MODULAR PLATE FIXATION SYSTEM FDA UDI
Generic Name
Bone-screw internal spinal fixation system, non-sterile FDA UDI
Model / Reference
8607-5535 FDA UDI

Identifiers

Catalog Number
8607-5535 FDA UDI
Primary DI / UDI-DI
00888480559801 FDA UDI
FDA Product Code
MAX FDA UDI
ODP FDA UDI
MQP FDA UDI
OVD FDA UDI
GMDN Term
Bone-screw internal spinal fixation system, non-sterile FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3080 FDA UDI
888.3060 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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

Category: Bone-screw internal spinal fixation system, non-sterile

Timberline Mpf Lateral Modular Plate Fixation System by Biomet Spine Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bone-screw internal spinal fixation system, non-sterile.

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 a3d4ad6c-befd-4475-88a8-b8b8fdaa701f 35 fields · synced Jun 8, 2026