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NEOTRACT ANCHOR

Page Type
Cleared 510(K)
510(k) Number
K061700
510(k) Type
Traditional
Applicant
Neotract, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/26/2006
Days to Decision
132 days
Submission Type
Summary

NEOTRACT ANCHOR

Page Type
Cleared 510(K)
510(k) Number
K061700
510(k) Type
Traditional
Applicant
Neotract, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/26/2006
Days to Decision
132 days
Submission Type
Summary