Atlas FDA

Crux Vena Cava Filter System, femoral; Crux Vena Cava Filter System, jugular

FDA 510(k) clearance K150262 · decided 2015-04-03

Clearance details

K-number
K150262
Device name
Crux Vena Cava Filter System, femoral; Crux Vena Cava Filter System, jugular
Applicant
Volcano Corporation
Decision
Substantially Equivalent
Date received
2015-02-04
Decision date
2015-04-03
Days to decision
58 days
Clearance type
Traditional
Product code
DTK
Device class
2
Regulation number
870.3375
Medical specialty
Cardiovascular
Advisory committee
Cardiovascular
Location
San Diego, CA, US
Third-party review
No
Expedited review
No

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Recalls involving this device

No recalls on record reference this clearance.