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MDI MII ONE-PIECE IMPLANT, 2.9MM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K081653
510(k) Type
Traditional
Applicant
IMTEC CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/19/2008
Days to Decision
99 days
Submission Type
Summary

MDI MII ONE-PIECE IMPLANT, 2.9MM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K081653
510(k) Type
Traditional
Applicant
IMTEC CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/19/2008
Days to Decision
99 days
Submission Type
Summary