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Polygon Resection Device

Page Type
Cleared 510(K)
510(k) Number
K182675
510(k) Type
Traditional
Applicant
Polygon Medical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/4/2019
Days to Decision
100 days
Submission Type
Summary

Polygon Resection Device

Page Type
Cleared 510(K)
510(k) Number
K182675
510(k) Type
Traditional
Applicant
Polygon Medical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/4/2019
Days to Decision
100 days
Submission Type
Summary