FDA 510(k) Applications Submitted by Cardiovascular System, Inc.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K151260 | 05/12/2015 | ViperWire Advance Guide Wire, Diamondback 360 Peripheral Orbital Atherectomy System, Stealth 360 Orbital PAD | Cardiovascular System, Inc. |
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