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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