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KISSloc Suture System

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