Reunion Rsa Shoulder System
FDA 510(k) K130895 · Howmedica Osteonics Corp.
510(k) numberK130895
Submission
- Device name
- Reunion Rsa Shoulder System
- Applicant
- Howmedica Osteonics Corp.
Mahwah, NJ, US - Received
- April 1, 2013
- Decision date
- December 27, 2013
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- PHX – Shoulder Prosthesis, Reverse Configuration
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 888.3660
- Specialty
- Orthopedic
- Implant
- Yes
Intended to be used to relieve pain and to replace the glenoid and humeral side of the shoulder joint in order to restore mobility in a grossly rotator cuff deficient joint with severe arthropathy or a previous joint replacement with a grossly rotator cuff deficient joint.
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| K253992 | Veritas Reverse Total Shoulder SystemPHX · Traditional | Restor3D | 05/07/2026SE |
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| K254128 | InSet Reverse Total Shoulder SystemPHX · Traditional | Shoulder Innovations, Inc. | 04/13/2026SE |
| K253674 | Blueprint Patient-Specific InstrumentationPHX · Traditional | Stryker Corporation (Tornier, S.A.S.) | 04/03/2026SE |
| K253624 | INHANCE Reverse Shoulder SystemPHX · Traditional | Depuy Ireland UC | 03/11/2026SE |
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Questions and answers
When was Reunion Rsa Shoulder System cleared by the FDA?
Reunion Rsa Shoulder System (K130895) received a 510(k) decision of Substantially Equivalent on December 27, 2013, 270 days after the submission was received.
What is the product code of K130895?
The FDA product code is PHX – Shoulder Prosthesis, Reverse Configuration, a Class II (moderate risk) device regulated under 21 CFR 888.3660.