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SECURE IMPLANT SYSTEM (2.5/3.0MM)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K080129
510(k) Type
Traditional
Applicant
Dio Department Dsi, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/30/2008
Days to Decision
134 days
Submission Type
Summary

SECURE IMPLANT SYSTEM (2.5/3.0MM)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K080129
510(k) Type
Traditional
Applicant
Dio Department Dsi, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/30/2008
Days to Decision
134 days
Submission Type
Summary