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ARTHREX CROSSPIN, MODEL AR-1964P

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K063719
510(k) Type
Traditional
Applicant
Arthrex, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/6/2007
Days to Decision
81 days
Submission Type
Summary

ARTHREX CROSSPIN, MODEL AR-1964P

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K063719
510(k) Type
Traditional
Applicant
Arthrex, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/6/2007
Days to Decision
81 days
Submission Type
Summary