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RESTORE BUNION CORRECTION SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K131061
510(k) Type
Traditional
Applicant
Nextremity Solutions
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/28/2013
Days to Decision
134 days
Submission Type
Summary

RESTORE BUNION CORRECTION SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K131061
510(k) Type
Traditional
Applicant
Nextremity Solutions
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/28/2013
Days to Decision
134 days
Submission Type
Summary