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SYNTHES 2.7MM AND 3.5MM VARIABLE ANGLE LCP MIDFOOT/HINDFOOT SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K131186
510(k) Type
Traditional
Applicant
Synthes (USA) Products, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/8/2013
Days to Decision
166 days
Submission Type
Summary

SYNTHES 2.7MM AND 3.5MM VARIABLE ANGLE LCP MIDFOOT/HINDFOOT SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K131186
510(k) Type
Traditional
Applicant
Synthes (USA) Products, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/8/2013
Days to Decision
166 days
Submission Type
Summary