Last synced on 30 November 2024 at 11:09 am

ANCHORAGE CLOSURE DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K073096
510(k) Type
Traditional
Applicant
EPITEK, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/7/2008
Days to Decision
98 days
Submission Type
Summary

ANCHORAGE CLOSURE DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K073096
510(k) Type
Traditional
Applicant
EPITEK, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/7/2008
Days to Decision
98 days
Submission Type
Summary