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USTAR II Knee System

FDA UDI

Class II (US FDA UDI)

by United Orthopedic Corp.

Identity

Trade Name
USTAR II Knee System FDA UDI
Generic Name
Knee tibia prosthesis trial, reusable FDA UDI
Device Name
USTAR II Yoke adaptor, M, fixed FDA UDI
Model / Reference
9415-9301-TB FDA UDI
Description
USTAR II Yoke adaptor, M, fixed FDA UDI

Identifiers

Catalog Number
9415-9301-TB FDA UDI
Primary DI / UDI-DI
04719872142560 FDA UDI
510(k) Number
K190100 FDA UDI
FDA Product Code
LPH FDA UDI
KRO FDA UDI
LWJ FDA UDI
KWL FDA UDI
GMDN Term
Knee tibia prosthesis trial, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3358 FDA UDI
888.3510 FDA UDI
888.3360 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

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Knee tibia prosthesis trial, reusable

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

Similar devices

Also classified as Knee tibia prosthesis trial, reusable.

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 1a22ca2b-b1b7-4caa-b62d-6199a8894de7 36 fields · synced May 30, 2026