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HOFFMANN LRF (LIMB RECONSTRUCTION FRAME) SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K130907
510(k) Type
Traditional
Applicant
Stryker Trauma AG
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/10/2013
Days to Decision
70 days
Submission Type
Summary

HOFFMANN LRF (LIMB RECONSTRUCTION FRAME) SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K130907
510(k) Type
Traditional
Applicant
Stryker Trauma AG
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/10/2013
Days to Decision
70 days
Submission Type
Summary