← Back to catalogue

Attune Lps

FDA UDI

Class II (US FDA UDI)

by Depuy (ireland)

Identity

Trade Name
ATTUNE LPS FDA UDI
Generic Name
Rotating hinged total knee prosthesis FDA UDI
Device Name
ATTUNE Knee System Revision LPS Insert AOX 24mm Medium FDA UDI
Model / Reference
1517-60-624 FDA UDI
Description
ATTUNE Knee System Revision LPS Insert AOX 24mm Medium FDA UDI

Identifiers

Catalog Number
151760624 FDA UDI
Primary DI / UDI-DI
10603295490821 FDA UDI
FDA Product Code
KRO FDA UDI
GMDN Term
Rotating hinged total knee prosthesis FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3510 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: Rotating hinged total knee prosthesis

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

Similar devices

Also classified as Rotating hinged total knee prosthesis.

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

Manufacturer
Depuy (ireland)

Sources (1)

  • FDA UDI 036ef5e9-e5ea-4158-8298-0007223aee37 35 fields · synced Jun 6, 2026