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MOTO Lateral Partial Knee System

FDA UDI

Class II (US FDA UDI)

by Medacta International

Identity

Trade Name
MOTO Lateral Partial Knee System FDA UDI
Generic Name
Uncoated unicondylar knee tibia prosthesis, polyethylene FDA UDI
Device Name
Size #5, 12mm thickness, LLRL FDA UDI
Model / Reference
02.18.IF5.12.LLRL FDA UDI
Description
Size #5, 12mm thickness, LLRL FDA UDI

Identifiers

Primary DI / UDI-DI
07630040721004 FDA UDI
510(k) Number
K183029 FDA UDI
FDA Product Code
HSX FDA UDI
GMDN Term
Uncoated unicondylar knee tibia prosthesis, polyethylene FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3520 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 unicondylar knee tibia prosthesis, polyethylene

MOTO Lateral Partial Knee System by Medacta International — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Uncoated unicondylar knee tibia prosthesis, polyethylene.

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 5fb2f258-74b7-45cb-8063-d04ee9176e93 34 fields · synced Jun 1, 2026