← Back to catalogue

U2 Total Knee System

FDA UDI

Class II (US FDA UDI)

by United Orthopedic Corp.

Identity

Trade Name
U2 Total Knee System FDA UDI
Generic Name
Cruciate-retaining total knee prosthesis FDA UDI
Device Name
Tibial Extension Stem, Ø12.5×35mm FDA UDI
Model / Reference
2703-7212 FDA UDI
Description
Tibial Extension Stem, Ø12.5×35mm FDA UDI

Identifiers

Primary DI / UDI-DI
04719886891003 FDA UDI
510(k) Number
K221705 FDA UDI
FDA Product Code
MBH FDA UDI
JWH FDA UDI
GMDN Term
Cruciate-retaining total knee prosthesis FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3565 FDA UDI
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: Posterior-stabilized total knee prosthesisCruciate-retaining total knee prosthesis

U2 Total Knee System by United Orthopedic Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Cruciate-retaining total knee prosthesis.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 4f7ab8af-3b91-4840-8a35-3e38c79934f5 35 fields · synced May 31, 2026