Last synced on 18 April 2025 at 11:05 pm

GRYPHON T BR DS ANCHOR W/ORTHOCORD, GRYPHON T BR ANCHOR W /ORTHOCORD, GRYPHON P BR DS ANCHOR W/ORTHOCORD, GRYPHON P BR A

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K100012
510(k) Type
Traditional
Applicant
DEPUY MITEK, A JOHNSON & JOHNSON COMPANY
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/30/2010
Days to Decision
116 days
Submission Type
Summary

GRYPHON T BR DS ANCHOR W/ORTHOCORD, GRYPHON T BR ANCHOR W /ORTHOCORD, GRYPHON P BR DS ANCHOR W/ORTHOCORD, GRYPHON P BR A

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K100012
510(k) Type
Traditional
Applicant
DEPUY MITEK, A JOHNSON & JOHNSON COMPANY
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/30/2010
Days to Decision
116 days
Submission Type
Summary