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INNERDYNE RADIALLY EXPANDING DILATION, RED DEVICE

Page Type
Cleared 510(K)
510(k) Number
K990854
510(k) Type
Traditional
Applicant
INNERDYNE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/2/1999
Days to Decision
140 days
Submission Type
Summary

INNERDYNE RADIALLY EXPANDING DILATION, RED DEVICE

Page Type
Cleared 510(K)
510(k) Number
K990854
510(k) Type
Traditional
Applicant
INNERDYNE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/2/1999
Days to Decision
140 days
Submission Type
Summary