Last synced on 9 May 2025 at 11:05 pm

BIORETEC ACTIVASCREW, ACTIVASCREW CANNULATED AND ACTIVASCREW CANNULATED WITH ACTIVAPIN

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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