FDA 510(k) Applications Submitted by Peter D O'Neill
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K151568 | 06/10/2015 | Arthrex OrthoVis Preoperative Plan | Custom Orthopaedic Solutions, Inc. |
| K151500 | 06/04/2015 | Arthrex Glenoid Intelligent Reusable Instrument System (Arthrex Glenoid IRIS) | CUSTOM ORTHOPAEDIC SOLUTIONS |
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