AGILON XO Shoulder System
FDA 510(k) K222482 · Implantcast GmbH
510(k) numberK222482
Submission
- Device name
- AGILON XO Shoulder System
- Applicant
- Implantcast GmbH
Buxtehude, DE - Received
- August 17, 2022
- Decision date
- September 28, 2022
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- KWT – Prosthesis, Shoulder, Non-Constrained, Metal/Polymer Cemented
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 888.3650
- Specialty
- Orthopedic
- Implant
- Yes
Other 510(k)s with product code KWT
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K262173 | N22 Offset Humeral HeadKWT · Traditional | Shoulder Innovations, Inc. | 09/08/2026SE |
| K250713 | Equinoxe® Humeral Reconstruction Prosthesis; Equinoxe® Stemless Shoulder ImplantsKWT · Traditional | Exactech, Inc. | 12/01/2025SE |
| K251686 | Tornier Humeral Reconstruction System Max (Tornier HRS Max)KWT · Traditional | Tornier, Inc. | 10/30/2025SE |
| K241944 | AGILON® XO Shoulder Replacement SystemKWT · Traditional | Implantcast GmbH | 03/10/2025SE |
| K241817 | InSet Total Shoulder SystemKWT · Traditional | Shoulder Innovations, Inc. | 02/11/2025SE |
| K231657 | AGILON® XO Shoulder Replacement SystemKWT · Traditional | Implantcast GmbH | 02/16/2024SE |
| K223631 | Comprehensive Segmental Revision System(SRS)KWT · Traditional | Biomet Orthopedics | 07/12/2023SE |
| K210899 | LINK Embrace Shoulder System- Anatomical ConfigurationKWT · Traditional | Waldemar Link GmbH & Co. KG | 06/21/2021SE |
| K191698 | TiN Coated Humeral HeadKWT · Traditional | Fx Shoulder USA, Inc. | 07/16/2020SE |
| K192365 | Shoulder Innovations Total Shoulder SystemKWT · Special | Shoulder Innovations, Inc. | 11/29/2019SE |
More from Shoulder Innovations, Inc.
| 510(k) | Device | Decision |
|---|---|---|
| K252451 | EPORE® XO cup systemOQI · Traditional | 04/24/2026SE |
| K260037 | implantcast Packaging System UpdateLZO · Traditional | 03/30/2026SE |
| K252401 | implaFit® short stemsLZO · Traditional | 03/12/2026SE |
| K241944 | AGILON® XO Shoulder Replacement SystemKWT · Traditional | 03/10/2025SE |
| K240391 | MUTARS® femoral stem cemented 160 mm and 200 mmLZO · Traditional | 10/24/2024SE |
| K234044 | ACS® LD FB Knee SystemJWH · Traditional | 09/06/2024SE |
| K240834 | EcoFit® short stem cementless cpTiLZO · Traditional | 06/03/2024SE |
| K231657 | AGILON® XO Shoulder Replacement SystemKWT · Traditional | 02/16/2024SE |
| K232371 | Actinia® hip stemsLZO · Traditional | 10/19/2023SE |
| K223103 | BethaLoc® stem cementless HALZO · Traditional | 06/20/2023SE |
Questions and answers
When was AGILON XO Shoulder System cleared by the FDA?
AGILON XO Shoulder System (K222482) received a 510(k) decision of Substantially Equivalent on September 28, 2022, 42 days after the submission was received.
What is the product code of K222482?
The FDA product code is KWT – Prosthesis, Shoulder, Non-Constrained, Metal/Polymer Cemented, a Class II (moderate risk) device regulated under 21 CFR 888.3650.