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AESCULAP STERNUMFIX STERNAL CLOSURE SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K063017
510(k) Type
Traditional
Applicant
AESCULAP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/27/2006
Days to Decision
86 days
Submission Type
Summary

AESCULAP STERNUMFIX STERNAL CLOSURE SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K063017
510(k) Type
Traditional
Applicant
AESCULAP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/27/2006
Days to Decision
86 days
Submission Type
Summary