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PENUMBRA EMBOLIZATION COIL SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K103305
510(k) Type
Traditional
Applicant
PENUMBRA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/26/2011
Days to Decision
78 days
Submission Type
Summary

PENUMBRA EMBOLIZATION COIL SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K103305
510(k) Type
Traditional
Applicant
PENUMBRA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/26/2011
Days to Decision
78 days
Submission Type
Summary