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Attune

FDA UDI

Class II (US FDA UDI)

by Depuy (ireland)

Identity

Trade Name
ATTUNE FDA UDI
Generic Name
Tibial insert FDA UDI
Device Name
ATTUNE KNEE SYSTEM TIBIAL INSERT FIXED BEARING MEDIAL STABILIZED LEFT AOX 4, 10mm FDA UDI
Model / Reference
1518-20-410 FDA UDI
Description
ATTUNE KNEE SYSTEM TIBIAL INSERT FIXED BEARING MEDIAL STABILIZED LEFT AOX 4, 10mm FDA UDI

Identifiers

Catalog Number
151820410 FDA UDI
Primary DI / UDI-DI
10603295541608 FDA UDI
510(k) Number
K211609 FDA UDI
FDA Product Code
MBH FDA UDI
JWH FDA UDI
OIY FDA UDI
GMDN Term
Tibial insert FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3565 FDA UDI
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: Tibial insert

Attune by Depuy (ireland) — 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

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Manufacturer

Manufacturer
Depuy (ireland)

Sources (1)

  • FDA UDI ec71e572-e8d9-4c7c-94a0-aa44d2a59197 36 fields · synced Jun 6, 2026