Free-Lock®

FDA UDI

Class II (US FDA UDI)

by Zimmer, Inc.

Identity

Trade Name: Free-Lock® FDA UDI
Generic Name: Orthopaedic fixation plate, non-bioabsorbable FDA UDI
Model / Reference: 1181-150-02 FDA UDI

Identifiers

Catalog Number: 00-1181-150-02 FDA UDI
Primary DI / UDI-DI: 00889024035515 FDA UDI
510(k) Number: K150818 FDA UDI
K830196 FDA UDI
FDA Product Code: KTT FDA UDI
GMDN Term: Orthopaedic fixation plate, non-bioabsorbable FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 888.3030 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

Yes

FDA UDI

Manufacturing Date

FDA UDI

Dimensions & Sizes

Size: Length — 59 Millimeter FDA UDI
Angle — 150 degree FDA UDI

Category: Orthopaedic fixation plate, non-bioabsorbable

Free-Lock® by Zimmer, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Cleared under the same submission

K150818 also covers:

K830196 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: Zimmer, Inc.

Sources (1)

FDA UDI cf90a23c-187c-456b-ad31-4ece4cda68e6 36 fields · synced Jun 8, 2026