FDA 510(k) Applications Submitted by Kelly Stratton
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K190556 | 03/05/2019 | Zimmer Biomet Universal Navigation System | Zimmer Biomet Spine, Inc. |
| K171907 | 06/26/2017 | Vitality« Spinal Fixation System | Zimmer Biomet Spine, Inc. |
| K172275 | 07/28/2017 | Vitality« Spinal Fixation System, Vitality«+ Power Instrument System | Zimmer Biomet Spine, Inc. |
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