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KISSloc Suture System

Page Type
Cleared 510(K)
510(k) Number
K170440
510(k) Type
Traditional
Applicant
Arthrosurface, Inc
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/3/2017
Days to Decision
78 days
Submission Type
Summary

KISSloc Suture System

Page Type
Cleared 510(K)
510(k) Number
K170440
510(k) Type
Traditional
Applicant
Arthrosurface, Inc
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/3/2017
Days to Decision
78 days
Submission Type
Summary