MTS Knee

FDA UDI

Class II (US FDA UDI)

by Medtronic, Inc.

Identity

Trade Name: MTS Knee FDA UDI
Generic Name: Joint prosthesis implantation kit, reusable FDA UDI
Device Name: DRILL 90-SRK-400013 PATELLA LUG FDA UDI
Model / Reference: 90-SRK-400013 FDA UDI
Description: DRILL 90-SRK-400013 PATELLA LUG FDA UDI

Identifiers

Primary DI / UDI-DI: 00763000201067 FDA UDI
FDA Product Code: JWH FDA UDI
GMDN Term: Joint prosthesis implantation kit, reusable FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 888.3560 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

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

Yes

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: Joint prosthesis implantation kit, reusable

MTS Knee by Medtronic, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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PROPHECY — MicroPort Orthopedics Inc. · Class II

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: Medtronic, Inc.

Sources (1)

FDA UDI 95c7f0ae-c3f2-4b76-ad1c-be9bc2466be2 34 fields · synced Jun 8, 2026