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Consensus Knee System

FDA UDI

Class II (US FDA UDI)

by Shalby Advanced Technologies, Inc.

Identity

Trade Name
Consensus Knee System FDA UDI
Generic Name
Coated knee tibia prosthesis FDA UDI
Device Name
Tibial Baseplate, Stemmed, Cementless, PC, L, 0 FDA UDI
Model / Reference
2781-0-0000 FDA UDI
Description
Tibial Baseplate, Stemmed, Cementless, PC, L, 0 FDA UDI

Identifiers

Catalog Number
2781-0-0000 FDA UDI
Primary DI / UDI-DI
00840286835299 FDA UDI
FDA Product Code
JWH FDA UDI
GMDN Term
Coated knee tibia prosthesis 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

Yes

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: Coated knee tibia prosthesis

Consensus Knee System by Shalby Advanced Technologies, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Coated knee tibia prosthesis.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 9c81d997-b568-4643-8dc0-98424b302cca 35 fields · synced May 29, 2026