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HOFFMANN LRF (LIMB RECONSTRUCTION FRAME) SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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