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Attune

FDA UDI

Class II (US FDA UDI)

by Depuy (ireland)

Identity

Trade Name
ATTUNE FDA UDI
Generic Name
Uncoated knee tibia prosthesis, metallic FDA UDI
Device Name
ATTUNE KNEE SYSTEM TIBIAL BASE FIXED BEARING SIZE 7 CEMENTED FDA UDI
Model / Reference
1506-00-007 FDA UDI
Description
ATTUNE KNEE SYSTEM TIBIAL BASE FIXED BEARING SIZE 7 CEMENTED FDA UDI

Identifiers

Catalog Number
150600007 FDA UDI
Primary DI / UDI-DI
10603295042419 FDA UDI
510(k) Number
K101433 FDA UDI
K233980 FDA UDI
FDA Product Code
JWH FDA UDI
OIY FDA UDI
GMDN Term
Uncoated knee tibia 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
MRI Safety
MR Conditional FDA UDI

Category: Uncoated knee tibia prosthesis, metallic

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

Similar devices

Also classified as Uncoated knee tibia prosthesis, metallic.

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 9a87a2c3-1188-4cfc-91ba-6f7a2e8ac435 36 fields · synced Jun 6, 2026