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CrossBow Fascial Closure System, CrossBow Fascial Closure System with Adaptor

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K172666
510(k) Type
Traditional
Applicant
Sutureease, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/1/2017
Days to Decision
87 days
Submission Type
Summary

CrossBow Fascial Closure System, CrossBow Fascial Closure System with Adaptor

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K172666
510(k) Type
Traditional
Applicant
Sutureease, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/1/2017
Days to Decision
87 days
Submission Type
Summary