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Quattro Bolt Tenodesis Screw

Page Type
Cleared 510(K)
510(k) Number
K143392
510(k) Type
Traditional
Applicant
CAYENNE MEDICAL, INC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/23/2015
Days to Decision
58 days
Submission Type
Summary

Quattro Bolt Tenodesis Screw

Page Type
Cleared 510(K)
510(k) Number
K143392
510(k) Type
Traditional
Applicant
CAYENNE MEDICAL, INC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/23/2015
Days to Decision
58 days
Submission Type
Summary