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CrossBow Fascial Closure System, CrossBow Fascial Closure System with Adaptor

Page Type
Cleared 510(K)
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)
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