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CoreHip® System

Page Type
Cleared 510(K)
510(k) Number
K172235
510(k) Type
Traditional
Applicant
Aesculap Implants Systems, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/28/2018
Days to Decision
246 days
Submission Type
Summary

CoreHip® System

Page Type
Cleared 510(K)
510(k) Number
K172235
510(k) Type
Traditional
Applicant
Aesculap Implants Systems, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/28/2018
Days to Decision
246 days
Submission Type
Summary