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ACTIVASCREW

Page Type
Cleared 510(K)
510(k) Number
K072848
510(k) Type
Special
Applicant
BIORETEC LTD
Country
Finland
FDA Decision
Substantially Equivalent
Decision Date
11/2/2007
Days to Decision
29 days
Submission Type
Summary

ACTIVASCREW

Page Type
Cleared 510(K)
510(k) Number
K072848
510(k) Type
Special
Applicant
BIORETEC LTD
Country
Finland
FDA Decision
Substantially Equivalent
Decision Date
11/2/2007
Days to Decision
29 days
Submission Type
Summary