INTERLOCK - 18 FIBERED IDC OCCLUSION SYSTEM
FDA 510(k) clearance K132578 · decided 2013-09-13
Clearance details
- K-number
- K132578
- Device name
- INTERLOCK - 18 FIBERED IDC OCCLUSION SYSTEM
- Applicant
- Boston Scientific Corp
- Decision
- Substantially Equivalent
- Date received
- 2013-08-16
- Decision date
- 2013-09-13
- Days to decision
- 28 days
- Clearance type
- Special
- Product code
- KRD
- Device class
- 2
- Regulation number
- 870.3300
- Medical specialty
- Cardiovascular
- Advisory committee
- Cardiovascular
- Location
- Maple Grove, MN, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.