Last synced on 31 March 2023 at 11:04 pm

ARTHREX FIBERWIRE, USP SIZE 5, MODEL AR-7201

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K012923
510(k) Type
Traditional
Applicant
ARTHREX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/4/2001
Days to Decision
34 days
Submission Type
Summary

ARTHREX FIBERWIRE, USP SIZE 5, MODEL AR-7201

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K012923
510(k) Type
Traditional
Applicant
ARTHREX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/4/2001
Days to Decision
34 days
Submission Type
Summary