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Evolis Total Knee System

FDA UDI

Class II (US FDA UDI)

by Medacta International

Identity

Trade Name
Evolis Total Knee System FDA UDI
Generic Name
Uncoated knee femur prosthesis, metallic FDA UDI
Device Name
Standard cemented femur size 6 left FDA UDI
Model / Reference
3010.206G FDA UDI
Description
Standard cemented femur size 6 left FDA UDI

Identifiers

Primary DI / UDI-DI
07630030844690 FDA UDI
510(k) Number
K081023 FDA UDI
FDA Product Code
JWH FDA UDI
GMDN Term
Uncoated knee femur prosthesis, metallic 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

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Uncoated knee femur prosthesis, metallic

Evolis Total Knee System by Medacta International — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Uncoated knee femur prosthesis, metallic.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 64071d04-3928-4de4-963a-a068f988c782 34 fields · synced May 31, 2026