Last synced on 30 September 2022 at 11:05 pm

RELIATACK ARTICULATING RELOADABLE FIXATION DEVICE WITH STANDARD PURCHASE ABSORBLE TACKS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K140609
510(k) Type
Special
Applicant
COVIDIEN
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/9/2014
Days to Decision
30 days
Submission Type
Summary

RELIATACK ARTICULATING RELOADABLE FIXATION DEVICE WITH STANDARD PURCHASE ABSORBLE TACKS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K140609
510(k) Type
Special
Applicant
COVIDIEN
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/9/2014
Days to Decision
30 days
Submission Type
Summary