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GII QUICKANCHOR PLUS WITH ORTHOCORD SUTURE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K051989
510(k) Type
Special
Applicant
DEPUY MITEK, A JOHNSON & JOHNSON COMPANY
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/5/2005
Days to Decision
14 days
Submission Type
Summary

GII QUICKANCHOR PLUS WITH ORTHOCORD SUTURE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K051989
510(k) Type
Special
Applicant
DEPUY MITEK, A JOHNSON & JOHNSON COMPANY
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/5/2005
Days to Decision
14 days
Submission Type
Summary