Last synced on 14 November 2025 at 11:06 pm

PROGENIX

Page Type
Cleared 510(K)
510(k) Number
K082463
510(k) Type
Traditional
Applicant
Medtronic Sofamor Danek
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/10/2008
Days to Decision
75 days
Submission Type
Summary

PROGENIX

Page Type
Cleared 510(K)
510(k) Number
K082463
510(k) Type
Traditional
Applicant
Medtronic Sofamor Danek
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/10/2008
Days to Decision
75 days
Submission Type
Summary