← Back to catalogue

Agility

FDA UDI

Class II (US FDA UDI)

by Depuy Orthopaedics, Inc.

Identity

Trade Name
AGILITY FDA UDI
Generic Name
Ankle prosthesis bearing FDA UDI
Device Name
AGILITY TOTAL ANKLE SYSTEM ANKLE INSERT SIZE 1 +2 FDA UDI
Model / Reference
1555-31-020 FDA UDI
Description
AGILITY TOTAL ANKLE SYSTEM ANKLE INSERT SIZE 1 +2 FDA UDI

Identifiers

Catalog Number
155531020 FDA UDI
Primary DI / UDI-DI
10603295058656 FDA UDI
510(k) Number
K020541 FDA UDI
K920802 FDA UDI
FDA Product Code
HSN FDA UDI
GMDN Term
Ankle prosthesis bearing 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: Ankle prosthesis bearing

Agility by Depuy Orthopaedics, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ankle prosthesis bearing.

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 65923638-c489-4713-8ba7-e45efac8ff39 36 fields · synced Jun 8, 2026