Device Classification Name |
catheter, peripheral, atherectomy
|
510(k) Number |
K151260 |
Device Name |
ViperWire Advance Guide Wire, Diamondback 360 Peripheral Orbital Atherectomy System, Stealth 360 Orbital PAD |
Applicant |
Cardiovascular System, Inc. |
1228 Old Highway 8 NW |
Saint Paul,
MN
55112
|
|
Applicant Contact |
Kim Wallner |
Correspondent |
Cardiovascular System, Inc. |
1228 Old Highway 8 NW |
Saint Paul,
MN
55112
|
|
Correspondent Contact |
Kim Wallner |
Regulation Number | 870.4875
|
Classification Product Code |
|
Date Received | 05/12/2015 |
Decision Date | 06/10/2015 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
Cardiovascular
|
510k Review Panel |
Cardiovascular
|
Summary |
Summary
|
Type |
Special
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
Recalls |
CDRH Recalls
|
|
|