FDA 510(k) Applications Submitted by ARTHROSURFACE INC.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K142942 | 10/14/2014 | HemiCAP Humeral Head XL (HHXL) Articular Resurfacing System | ARTHROSURFACE INC. |
| K203375 | 11/16/2020 | OVOMotion Reverse Shoulder Arthroplasty System | Arthrosurface Inc. |
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