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Ortho Device, ADAPTIX 3D Orthopedic Imaging System

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K221949
510(k) Type
Traditional
Applicant
Pausch Medical GmbH
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
1/26/2023
Days to Decision
205 days
Submission Type
Summary

Ortho Device, ADAPTIX 3D Orthopedic Imaging System

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K221949
510(k) Type
Traditional
Applicant
Pausch Medical GmbH
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
1/26/2023
Days to Decision
205 days
Submission Type
Summary