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ACTIVASCREW

Page Type
Cleared 510(K)
510(k) Number
K062980
510(k) Type
Traditional
Applicant
Bioretec , Ltd.
Country
Finland
FDA Decision
Substantially Equivalent
Decision Date
11/22/2006
Days to Decision
54 days
Submission Type
Summary

ACTIVASCREW

Page Type
Cleared 510(K)
510(k) Number
K062980
510(k) Type
Traditional
Applicant
Bioretec , Ltd.
Country
Finland
FDA Decision
Substantially Equivalent
Decision Date
11/22/2006
Days to Decision
54 days
Submission Type
Summary