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SUPERIOR LATERAL VARIAX CLAVICLE PLATE

Page Type
Cleared 510(K)
510(k) Number
K130116
510(k) Type
Special
Applicant
Stryker Trauma AG
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/5/2013
Days to Decision
48 days
Submission Type
Summary

SUPERIOR LATERAL VARIAX CLAVICLE PLATE

Page Type
Cleared 510(K)
510(k) Number
K130116
510(k) Type
Special
Applicant
Stryker Trauma AG
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/5/2013
Days to Decision
48 days
Submission Type
Summary