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CROSSFIX II MEMISCAL REPAIR DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K121413
510(k) Type
Special
Applicant
CAYENNE MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/4/2012
Days to Decision
24 days
Submission Type
Summary

CROSSFIX II MEMISCAL REPAIR DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K121413
510(k) Type
Special
Applicant
CAYENNE MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/4/2012
Days to Decision
24 days
Submission Type
Summary