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NEOTRACT ANCHOR SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K073651
510(k) Type
Traditional
Applicant
NEOTRACT, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/1/2008
Days to Decision
37 days
Submission Type
Summary

NEOTRACT ANCHOR SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K073651
510(k) Type
Traditional
Applicant
NEOTRACT, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/1/2008
Days to Decision
37 days
Submission Type
Summary