Last synced on 14 November 2025 at 11:06 pm

ENDODRAPE

Page Type
Cleared 510(K)
510(k) Number
K070406
510(k) Type
Traditional
Applicant
VORTEK SURGICAL, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/30/2007
Days to Decision
168 days
Submission Type
Summary

ENDODRAPE

Page Type
Cleared 510(K)
510(k) Number
K070406
510(k) Type
Traditional
Applicant
VORTEK SURGICAL, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/30/2007
Days to Decision
168 days
Submission Type
Summary