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ABSORBATACK 5MM SINGLE USE ABSORBABLE FIXATION DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K091900
510(k) Type
Special
Applicant
COVIDIEN LP, FORMERLY REGISTERED AS UNITED STATES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/16/2009
Days to Decision
21 days
Submission Type
Summary

ABSORBATACK 5MM SINGLE USE ABSORBABLE FIXATION DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K091900
510(k) Type
Special
Applicant
COVIDIEN LP, FORMERLY REGISTERED AS UNITED STATES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/16/2009
Days to Decision
21 days
Submission Type
Summary