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Natural-Knee®

FDA UDI

Class II (US FDA UDI)

by Zimmer, Inc.

Identity

Trade Name
Natural-Knee® FDA UDI
Generic Name
Patella prosthesis trial FDA UDI
Model / Reference
6226-01-000 FDA UDI

Identifiers

Catalog Number
6226-01-000 FDA UDI
Primary DI / UDI-DI
00889024254053 FDA UDI
510(k) Number
K002335 FDA UDI
K936159 FDA UDI
FDA Product Code
JWH FDA UDI
GMDN Term
Patella prosthesis trial 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

No

FDA UDI

Single Use

No

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: Patella prosthesis trial

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

Similar devices

Also classified as Patella prosthesis trial.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Zimmer, Inc.

Sources (1)

  • FDA UDI de731366-574e-46fa-8cdf-ddb01b8d6944 36 fields · synced May 30, 2026