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AESCULAP BIPOLAR ACETABULAR CUP

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K060707
510(k) Type
Traditional
Applicant
Aesculap, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/31/2006
Days to Decision
76 days
Submission Type
Summary

AESCULAP BIPOLAR ACETABULAR CUP

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K060707
510(k) Type
Traditional
Applicant
Aesculap, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/31/2006
Days to Decision
76 days
Submission Type
Summary