The following data is part of a premarket notification filed by Volcano Atheromed Inc. with the FDA for Phoenix 2.4mm Atherectomy Plus System.
Device ID | K181877 |
510k Number | K181877 |
Device Name: | Phoenix 2.4mm Atherectomy Plus System |
Classification | Catheter, Peripheral, Atherectomy |
Applicant | Volcano AtheroMed Inc. 1530 O'Brien Drive Suite A Menlo Park, CA 94025 |
Contact | Jean Chang |
Correspondent | Jean Chang Volcano AtheroMed Inc. 1530 O'Brien Drive Suite A Menlo Park, CA 94025 |
Product Code | MCW |
CFR Regulation Number | 870.4875 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2018-07-13 |
Decision Date | 2018-12-17 |
Summary: | summary |