Catalyst CSR Press-Fit Humeral Components
FDA 510(k) K182500 · Catalyst Orthoscience, Inc.
510(k) numberK182500
Submission
- Device name
- Catalyst CSR Press-Fit Humeral Components
- Applicant
- Catalyst Orthoscience, Inc.
Naples, FL, US - Received
- September 12, 2018
- Decision date
- January 11, 2019
- 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 |
| K222482 | AGILON XO Shoulder SystemKWT · Traditional | Implantcast GmbH | 09/28/2022SE |
| 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 |
More from Fx Shoulder USA, Inc.
| 510(k) | Device | Decision |
|---|---|---|
| K252418 | Catalyst F1x Shoulder SystemKWS · Traditional | 11/06/2025SE |
| K234105 | Catalyst F1x Shoulder SystemPHX · Traditional | 04/05/2024SE |
| K232583 | Catalyst R1 Reverse Shoulder SystemPHX · Special | 09/20/2023SE |
| K223655 | Catalyst R1 Reverse Shoulder SystemPHX · Traditional | 05/09/2023SE |
| K222317 | Catalyst EA Convertible Stemmed ShoulderKWS · Traditional | 11/10/2022SE |
| K213349 | Catalyst R1 Reverse Shoulder SystemPHX · Traditional | 06/23/2022SE |
| K211991 | Catalyst R1 Reverse Shoulder SystemPHX · Special | 07/28/2021SE |
| K202611 | Catalyst OrthoScience R1 Reverse Shoulder SystemPHX · Traditional | 02/12/2021SE |
| K191811 | Catalyst OrthoScience CSR Shoulder SystemKWT · Special | 09/11/2019SE |
| K181287 | Catalyst CSR Shoulder SystemKWT · Special | 07/12/2018SE |
Questions and answers
When was Catalyst CSR Press-Fit Humeral Components cleared by the FDA?
Catalyst CSR Press-Fit Humeral Components (K182500) received a 510(k) decision of Substantially Equivalent on January 11, 2019, 121 days after the submission was received.
What is the product code of K182500?
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.