Timx

FDA UDI

Class II (US FDA UDI)

by Depuy Spine, Inc.

Identity

Trade Name: TIMX FDA UDI
Generic Name: Spinal bone set screw FDA UDI
Device Name: TIMX LOW BACK SYSTEM SET SCREW-METRIC THREAD M7 9.30mm FDA UDI
Model / Reference: 325005SS FDA UDI
Description: TIMX LOW BACK SYSTEM SET SCREW-METRIC THREAD M7 9.30mm FDA UDI

Identifiers

Catalog Number: 325005SS FDA UDI
Primary DI / UDI-DI: 10705034241470 FDA UDI
510(k) Number: K953978 FDA UDI
FDA Product Code: KWQ FDA UDI
GMDN Term: Spinal bone set screw FDA UDI

Classification

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

Clinical & Handling

Sterile

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

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Spinal bone set screw

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

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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: Depuy Spine, Inc.

Sources (1)

FDA UDI e117d4c2-b173-4ce8-a5a3-a0c3255da66e 36 fields · synced May 30, 2026