STEALTH 360 ORBITAL PAD SYSTEM
FDA 510(k) clearance K122987 · decided 2012-10-25
Clearance details
- K-number
- K122987
- Device name
- STEALTH 360 ORBITAL PAD SYSTEM
- Applicant
- Cardiovascular Systems, Inc.
- Decision
- Substantially Equivalent
- Date received
- 2012-09-26
- Decision date
- 2012-10-25
- Days to decision
- 29 days
- Clearance type
- Special
- Product code
- MCW
- Device class
- 2
- Regulation number
- 870.4875
- Medical specialty
- Cardiovascular
- Advisory committee
- Cardiovascular
- Location
- Saint Paul, MN, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.