510(k) K093286
K093286 is an FDA 510(k) premarket notification submitted by Ev3, Inc. for the device "POWERCROSS .018 OTW PTA DILATION CATHETER". The FDA issued a decision of Substantially Equivalent on November 13, 2009. The device falls under product code LIT (Catheter, Angioplasty, Peripheral, Transluminal), a Class II device regulated under 21 CFR 870.1250. Ev3, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- November 13, 2009
- Date Received
- October 20, 2009
- Clearance Type
- Special
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Catheter, Angioplasty, Peripheral, Transluminal
- Device Class
- Class II
- Regulation Number
- 870.1250
- Review Panel
- CV
- Submission Type