Titan Reverse Shoulder System
FDA 510(k) K130050 · Ascension Orthopedic
510(k) numberK130050
Submission
- Device name
- Titan Reverse Shoulder System
- Applicant
- Ascension Orthopedic
Austin, TX, US - Received
- January 9, 2013
- Decision date
- June 18, 2013
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- KWS – Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 888.3660
- Specialty
- Orthopedic
- Implant
- Yes
Other 510(k)s with product code KWS
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K260721 | Tornier Perform Advanced GlenoidKWS · Traditional | Tornier, Inc. | 07/22/2026SE |
| K254084 | AETOS Shoulder System - CONCELOC GlenoidsKWS · Traditional | Smith & Nephew, Inc. | 04/06/2026SE |
| K252418 | Catalyst F1x Shoulder SystemKWS · Traditional | Catalyst Orthoscience, Inc. | 11/06/2025SE |
| K252416 | AETOS Shoulder System Meta Humeral Prosthesis Size 0KWS · Traditional | Smith & Nephew, Inc. | 10/29/2025SE |
| K241292 | MyShoulder Planner (5.3SSWPL)KWS · Traditional | Medacta International S.A. | 01/30/2025SE |
| K241878 | Tornier Humeral Reconstruction System (Tornier HRS); Tornier Perform Humeral System -…KWS · Traditional | Stryker Corporation (Tornier, Inc.) | 12/06/2024SE |
| K241609 | Tornier Humeral Reconstruction System (Tornier HRS)KWS · Traditional | Stryker Corporation (Tornier, Inc.) | 09/10/2024SE |
| K230513 | Arthrex Univers Apex OptiFit Humeral StemKWS · Traditional | Arthrex, Inc. | 09/26/2023SE |
| K222592 | AltiVate® Anatomic Shoulder AG e+ with MarkersKWS · Abbreviated | Encore Medical L.P. | 06/23/2023SE |
| K230572 | AETOS Shoulder SystemKWS · Traditional | Smith & Nephew, Inc. | 06/07/2023SE |
More from Smith & Nephew, Inc.
| 510(k) | Device | Decision |
|---|---|---|
| K140463 | Integra External Fixation SystemKTT · Traditional | 10/10/2014SE |
| K131360 | Integra Titanium Bone WedgeHRS · Traditional | 08/07/2013SE |
| K112438 | Titan Modular Total Shoulder SystemKWS · Special | 04/11/2012SE |
| K112481 | First Choice Druj System, Partial Head ImplantKXE · Traditional | 04/09/2012SE |
| K112278 | Ascension Nugrip CMC ImplantKYI · Traditional | 11/04/2011SE |
| K111799 | Nugait(Tm) Subtalar Implant SystemHWC · Traditional | 08/19/2011SE |
Questions and answers
When was Titan Reverse Shoulder System cleared by the FDA?
Titan Reverse Shoulder System (K130050) received a 510(k) decision of Substantially Equivalent on June 18, 2013, 160 days after the submission was received.
What is the product code of K130050?
The FDA product code is KWS – Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented, a Class II (moderate risk) device regulated under 21 CFR 888.3660.