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APTUS® Ankle Trauma System 2.8/3.5

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K193633
510(k) Type
Traditional
Applicant
Medartis AG
Country
Switzerland
FDA Decision
Substantially Equivalent
Decision Date
3/26/2020
Days to Decision
90 days
Submission Type
Summary

APTUS® Ankle Trauma System 2.8/3.5

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K193633
510(k) Type
Traditional
Applicant
Medartis AG
Country
Switzerland
FDA Decision
Substantially Equivalent
Decision Date
3/26/2020
Days to Decision
90 days
Submission Type
Summary