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PELVIS II IMPLANT SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K131132
510(k) Type
Traditional
Applicant
Stryker Trauma AG
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/31/2013
Days to Decision
38 days
Submission Type
Summary

PELVIS II IMPLANT SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K131132
510(k) Type
Traditional
Applicant
Stryker Trauma AG
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/31/2013
Days to Decision
38 days
Submission Type
Summary