FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
CRUX SNARE FILTER RETRIEVAL SET
K Number: K133681
·
Decision Jan 30, 2014
Classifications
1
FEI Numbers
36
Registration Numbers
36
Same Product Code
31
Applicant Total
55
Review Days
59
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Basic Information
- Device Name
- CRUX SNARE FILTER RETRIEVAL SET
- K Number
- K133681
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 870.5150
- Medical Specialty
- Cardiovascular
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Volcano Corporation
- Date Received
- December 2, 2013
- Decision Date
- January 30, 2014
- Product Code
- MMX
- Advisory Committee
- Cardiovascular
- Review Advisory Committee
- CV
- Third Party
- N
Classifications
This FDA 510(k) entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| MMX | Device, Percutaneous Retrieval | FDA class 2 | Cardiovascular |
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