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DePuy Actis DuoFix Hip Prosthesis

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K160907
510(k) Type
Traditional
Applicant
DEPUY (IRELAND)
Country
Ireland
FDA Decision
Substantially Equivalent
Decision Date
7/19/2016
Days to Decision
109 days
Submission Type
Summary

DePuy Actis DuoFix Hip Prosthesis

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K160907
510(k) Type
Traditional
Applicant
DEPUY (IRELAND)
Country
Ireland
FDA Decision
Substantially Equivalent
Decision Date
7/19/2016
Days to Decision
109 days
Submission Type
Summary