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ARTHREX WRIST BIO-ANCHOR, MODEL AR-1322B

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K022234
510(k) Type
Traditional
Applicant
ARTHREX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/3/2002
Days to Decision
84 days
Submission Type
Summary

ARTHREX WRIST BIO-ANCHOR, MODEL AR-1322B

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K022234
510(k) Type
Traditional
Applicant
ARTHREX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/3/2002
Days to Decision
84 days
Submission Type
Summary