The following data is part of a premarket notification filed by Cardiovascular Systems, Inc. with the FDA for Modification To: Diamondback 360 Orbital Atherectomy System.
| Device ID | K072748 |
| 510k Number | K072748 |
| Device Name: | MODIFICATION TO: DIAMONDBACK 360 ORBITAL ATHERECTOMY SYSTEM |
| Classification | Catheter, Peripheral, Atherectomy |
| Applicant | CARDIOVASCULAR SYSTEMS, INC. 18555 37TH AVE N Plymouth, MN 55446 |
| Contact | John Carline |
| Correspondent | John Carline CARDIOVASCULAR SYSTEMS, INC. 18555 37TH AVE N Plymouth, MN 55446 |
| Product Code | MCW |
| CFR Regulation Number | 870.4875 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2007-09-27 |
| Decision Date | 2007-11-09 |
| Summary: | summary |