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ARTHREX FIBERWIRE, MODEL SPU-02NB-3800

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K010673
510(k) Type
Traditional
Applicant
ARTHREX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/14/2001
Days to Decision
69 days
Submission Type
Summary

ARTHREX FIBERWIRE, MODEL SPU-02NB-3800

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K010673
510(k) Type
Traditional
Applicant
ARTHREX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/14/2001
Days to Decision
69 days
Submission Type
Summary