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Asnis III Cannulated Screw System, Asnis PRO Cannulated Screw System

Page Type
Cleared 510(K)
510(k) Number
K220319
510(k) Type
Traditional
Applicant
Stryker GmbH
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/10/2022
Days to Decision
127 days
Submission Type
Summary

Asnis III Cannulated Screw System, Asnis PRO Cannulated Screw System

Page Type
Cleared 510(K)
510(k) Number
K220319
510(k) Type
Traditional
Applicant
Stryker GmbH
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/10/2022
Days to Decision
127 days
Submission Type
Summary