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Double ENDOBUTTON Fixation Device

Page Type
Cleared 510(K)
510(k) Number
K183232
510(k) Type
Traditional
Applicant
Smith and Nephew, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/12/2019
Days to Decision
112 days
Submission Type
Summary

Double ENDOBUTTON Fixation Device

Page Type
Cleared 510(K)
510(k) Number
K183232
510(k) Type
Traditional
Applicant
Smith and Nephew, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/12/2019
Days to Decision
112 days
Submission Type
Summary