Last synced on 14 November 2025 at 11:06 pm

BIORETEC ACTIVASCREW INTERFERENCE

Page Type
Cleared 510(K)
510(k) Number
K130716
510(k) Type
Traditional
Applicant
BIORETEC LTD
Country
Finland
FDA Decision
Substantially Equivalent
Decision Date
8/28/2013
Days to Decision
166 days
Submission Type
Summary

BIORETEC ACTIVASCREW INTERFERENCE

Page Type
Cleared 510(K)
510(k) Number
K130716
510(k) Type
Traditional
Applicant
BIORETEC LTD
Country
Finland
FDA Decision
Substantially Equivalent
Decision Date
8/28/2013
Days to Decision
166 days
Submission Type
Summary