FDA 510(k) Applications Submitted by Scott Coleridge
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K221010 | 04/05/2022 | Intra.Ox 2.0 Handheld Tissue Oximeter | ViOptix, Inc. |
| K191676 | 06/24/2019 | Intra.Ox 2.0 Handheld Tissue Oximeter | ViOptix, Inc. |
| K153057 | 10/21/2015 | FitRiteÖ Total Hip Arthroplasty System | EXCERA ORTHOPEDICS, INC. |
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