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VariAx 2 Distal Radius System, VariAx 2 Distal Ulna System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K212581
510(k) Type
Traditional
Applicant
Stryker GmbH
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/19/2022
Days to Decision
156 days
Submission Type
Summary

VariAx 2 Distal Radius System, VariAx 2 Distal Ulna System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K212581
510(k) Type
Traditional
Applicant
Stryker GmbH
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/19/2022
Days to Decision
156 days
Submission Type
Summary