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BIORETEC ACTIVASCREW, ACTIVASCREW CANNULATED AND ACTIVASCREW CANNULATED WITH ACTIVAPIN

Page Type
Cleared 510(K)
510(k) Number
K081392
510(k) Type
Special
Applicant
Bioretec , Ltd.
Country
Finland
FDA Decision
Substantially Equivalent
Decision Date
6/18/2008
Days to Decision
30 days
Submission Type
Summary

BIORETEC ACTIVASCREW, ACTIVASCREW CANNULATED AND ACTIVASCREW CANNULATED WITH ACTIVAPIN

Page Type
Cleared 510(K)
510(k) Number
K081392
510(k) Type
Special
Applicant
Bioretec , Ltd.
Country
Finland
FDA Decision
Substantially Equivalent
Decision Date
6/18/2008
Days to Decision
30 days
Submission Type
Summary