ReUnion Reversible Fracture System (RFX), ReUnion Reverse Shoulder Arthroplasty System (RS — Stryker Trauma AG (510(k) K172210)
ReUnion Reversible Fracture System (RFX), ReUnion Reverse Shoulder Arthroplasty System (RS — Stryker Trauma AG (510(k) K172210) is one of 9,000 device clearances in the DeviceClear dataset. Key details — Device name: ReUnion Reversible Fracture System (RFX), ReUnion Reverse Shoulder Arthroplasty System (RS; Applicant:
| Device name | ReUnion Reversible Fracture System (RFX), ReUnion Reverse Shoulder Arthroplasty System (RS |
|---|---|
| Applicant | Stryker Trauma AG |
| Clearance track | 510(k) |
| Submission number | K172210 |
| Decision | Substantially Equivalent |
| Decision date | 2017-10-02 |
| Date received | 2017-07-24 |
| Product code | KWS |
| Device class | 2 |
| Medical specialty | Orthopedic |
| Applicant location | NJ, US |
| Source | openFDA device |
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$1999/mo
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