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PLANMECA PROMAX 3D

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K060328
510(k) Type
Traditional
Applicant
Planmeca Oy
Country
Finland
FDA Decision
Substantially Equivalent
Decision Date
3/15/2006
Days to Decision
34 days
Submission Type
Summary

PLANMECA PROMAX 3D

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K060328
510(k) Type
Traditional
Applicant
Planmeca Oy
Country
Finland
FDA Decision
Substantially Equivalent
Decision Date
3/15/2006
Days to Decision
34 days
Submission Type
Summary