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SPIDERX EMBOLIC PROTECTION DEVICE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K052659
510(k) Type
Traditional
Applicant
Ev3, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/17/2006
Days to Decision
143 days
Submission Type
Summary

SPIDERX EMBOLIC PROTECTION DEVICE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K052659
510(k) Type
Traditional
Applicant
Ev3, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/17/2006
Days to Decision
143 days
Submission Type
Summary