TURBOHAWK PERIPHERAL PLAQUE EXCISION SYSTEM
FDA 510(k) clearance K111723 · decided 2011-10-27
Clearance details
- K-number
- K111723
- Device name
- TURBOHAWK PERIPHERAL PLAQUE EXCISION SYSTEM
- Applicant
- Ev3, Inc.
- Decision
- Substantially Equivalent
- Date received
- 2011-06-20
- Decision date
- 2011-10-27
- Days to decision
- 129 days
- Clearance type
- Traditional
- Product code
- MCW
- Device class
- 2
- Regulation number
- 870.4875
- Medical specialty
- Cardiovascular
- Advisory committee
- Cardiovascular
- Location
- Plymouth, MN, US
- Third-party review
- No
- Expedited review
- No
+ Add to Predicate Builder ◉ Watch Ev3
Need this as data, not a web page?
Query all 176,000+ clearances through the Atlas FDA API, or subscribe to weekly change alerts. Self-serve from $29/mo.
Similar devices under this product code
Devices cleared under the same product code - the starting set for predicate research.
Recalls involving this device
No recalls on record reference this clearance.