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IXOS Radius Plate System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K171624
510(k) Type
Traditional
Applicant
Stuckenbrock Medizintechnik GmbH
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
3/29/2018
Days to Decision
300 days
Submission Type
Summary

IXOS Radius Plate System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K171624
510(k) Type
Traditional
Applicant
Stuckenbrock Medizintechnik GmbH
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
3/29/2018
Days to Decision
300 days
Submission Type
Summary