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Legion

FDA UDI

Class II (US FDA UDI)

by Smith & Nephew, Inc.

Identity

Trade Name
LEGION FDA UDI
Generic Name
Uncoated knee femur prosthesis, metallic FDA UDI
Device Name
LEGION CRUCIATE RETAINING NONPOROUS FEMORAL SIZE 8 LEFT FDA UDI
Model / Reference
71423208 FDA UDI
Description
LEGION CRUCIATE RETAINING NONPOROUS FEMORAL SIZE 8 LEFT FDA UDI

Identifiers

Catalog Number
71423208 FDA UDI
Primary DI / UDI-DI
00885556030943 FDA UDI
510(k) Number
K060742 FDA UDI
FDA Product Code
JWH FDA UDI
GMDN Term
Uncoated knee femur prosthesis, metallic 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

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 knee femur prosthesis, metallic

Legion by Smith & Nephew, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Uncoated knee femur prosthesis, metallic.

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 ac269a9d-cf41-49e4-920e-985fe0f7fc49 36 fields · synced Jun 8, 2026