← Back to catalogue

XT Revision Ankle Replacement System

FDA UDI

Class II (US FDA UDI)

by Smith & Nephew, Inc.

Identity

Trade Name
XT Revision Ankle Replacement System FDA UDI
Generic Name
Fixed-bearing total ankle prosthesis FDA UDI
Device Name
INTEGRA XT. INSERT. SIZE 0. LEFT. TH19 FDA UDI
Model / Reference
LJU232T FDA UDI
Description
INTEGRA XT. INSERT. SIZE 0. LEFT. TH19 FDA UDI

Identifiers

Catalog Number
LJU232T FDA UDI
Primary DI / UDI-DI
00885556840634 FDA UDI
510(k) Number
K153452 FDA UDI
FDA Product Code
HSN FDA UDI
GMDN Term
Fixed-bearing total ankle prosthesis FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3110 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: Fixed-bearing total ankle prosthesis

XT Revision Ankle Replacement System by Smith & Nephew, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Fixed-bearing total ankle prosthesis.

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 b50b3351-ecc7-472a-be54-0b3b91c6c670 36 fields · synced Jun 8, 2026