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GingiKnit+, GingiBraid+, and Shortcut with GingiBraid+ Non-Impregnated Retraction Cord

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K162164
510(k) Type
Traditional
Applicant
KERR CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/13/2017
Days to Decision
163 days
Submission Type
Summary

GingiKnit+, GingiBraid+, and Shortcut with GingiBraid+ Non-Impregnated Retraction Cord

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K162164
510(k) Type
Traditional
Applicant
KERR CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/13/2017
Days to Decision
163 days
Submission Type
Summary