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GAMMA3 AND T2 RECON TARGETING DEVICES

Page Type
Cleared 510(K)
510(k) Number
K123401
510(k) Type
Traditional
Applicant
Stryker Trauma AG
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/23/2013
Days to Decision
79 days
Submission Type
Summary

GAMMA3 AND T2 RECON TARGETING DEVICES

Page Type
Cleared 510(K)
510(k) Number
K123401
510(k) Type
Traditional
Applicant
Stryker Trauma AG
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/23/2013
Days to Decision
79 days
Submission Type
Summary