Last synced on 25 November 2022 at 11:04 pm

THE FIAGON NAVIGATION - EXTENDED INSTRUMENT SET ENT, REGISTRATIONPOINTER, VENTERAPOINTER, GUIDEWIRE, POINTERSHELL

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K141456
510(k) Type
Traditional
Applicant
FIAGON GMBH
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
10/8/2014
Days to Decision
128 days
Submission Type
Summary

THE FIAGON NAVIGATION - EXTENDED INSTRUMENT SET ENT, REGISTRATIONPOINTER, VENTERAPOINTER, GUIDEWIRE, POINTERSHELL

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K141456
510(k) Type
Traditional
Applicant
FIAGON GMBH
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
10/8/2014
Days to Decision
128 days
Submission Type
Summary