Last synced on 25 January 2026 at 3:41 am

GRYPHON P BR DS ANCHOR W/ORTHOCORD,GRYPHON P BR ANCHOR W/ORTHOCORD, MODEL 210813,210814

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K090124
510(k) Type
Special
Applicant
Depuy Mitek, A Johnson & Johnson Company
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/11/2009
Days to Decision
49 days
Submission Type
Summary

GRYPHON P BR DS ANCHOR W/ORTHOCORD,GRYPHON P BR ANCHOR W/ORTHOCORD, MODEL 210813,210814

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K090124
510(k) Type
Special
Applicant
Depuy Mitek, A Johnson & Johnson Company
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/11/2009
Days to Decision
49 days
Submission Type
Summary