Attune

FDA UDI

Class III (US FDA UDI)

by Depuy (ireland)

Identity

Trade Name: ATTUNE FDA UDI
Generic Name: Tibial insert FDA UDI
Device Name: ATTUNE KNEE SYSTEM REVISION CRS ROTATING PLATFORM INSERT AOX 22MM SIZE 3 FDA UDI
Model / Reference: 1517-10-322 FDA UDI
Description: ATTUNE KNEE SYSTEM REVISION CRS ROTATING PLATFORM INSERT AOX 22MM SIZE 3 FDA UDI

Identifiers

Catalog Number: 151710322 FDA UDI
Primary DI / UDI-DI: 10603295055761 FDA UDI
FDA Product Code: NJL FDA UDI
GMDN Term: Tibial insert FDA UDI

Classification

Device Class: Class III 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

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

MRI Safety

MR Conditional FDA UDI

Category: Tibial insert

Attune by Depuy (ireland) — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Also classified as Tibial insert.

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Maxim Knee System — Biomet Orthopedics, Inc. · Class II
Scorpio — Howmedica Osteonics Corp. · Class II
TriVerse Meniscal Insert PS+ — SIGNATURE ORTHOPAEDICS PTY LTD · Class II
Scorpio — Howmedica Osteonics Corp. · Class II
World Knee System — SIGNATURE ORTHOPAEDICS PTY LTD · Class II
Optetrak Logic — Exactech, Inc. · Class II

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class III	Pending data

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Manufacturer

Manufacturer: Depuy (ireland)

Sources (1)

FDA UDI 96e24054-7833-4dd3-ac10-b567329ef60a 35 fields · synced Jun 1, 2026