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PeriPRO™ Femur System, Variable Angle Fixation System, AxSOS 3Ti, Stryker Plating System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K222381
510(k) Type
Traditional
Applicant
Stryker GmbH
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/27/2023
Days to Decision
265 days
Submission Type
Summary

PeriPRO™ Femur System, Variable Angle Fixation System, AxSOS 3Ti, Stryker Plating System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K222381
510(k) Type
Traditional
Applicant
Stryker GmbH
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/27/2023
Days to Decision
265 days
Submission Type
Summary