← Back to catalogue

Legion

FDA UDI

Class II (US FDA UDI)

by Smith & Nephew, Inc.

Identity

Trade Name
LEGION FDA UDI
Generic Name
Tibial insert FDA UDI
Device Name
VKS CS INSERT W/ LEGION LOCK SIZE 3-4 17MM TRIAL FDA UDI
Model / Reference
71934369 FDA UDI
Description
VKS CS INSERT W/ LEGION LOCK SIZE 3-4 17MM TRIAL FDA UDI

Identifiers

Catalog Number
71934369 FDA UDI
Primary DI / UDI-DI
00885556006290 FDA UDI
510(k) Number
K951987 FDA UDI
FDA Product Code
JWH FDA UDI
GMDN Term
Tibial insert 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

No

FDA UDI

Single Use

No

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

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Tibial insert

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

Similar devices

Also classified as Tibial insert.

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 d92a5871-c5f1-41d1-9e3e-4457c89ad627 36 fields · synced Jun 6, 2026