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ARTHREX BIO-COMPRESSION SCREW

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K060478
510(k) Type
Traditional
Applicant
Arthrex, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/19/2006
Days to Decision
85 days
Submission Type
Summary

ARTHREX BIO-COMPRESSION SCREW

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K060478
510(k) Type
Traditional
Applicant
Arthrex, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/19/2006
Days to Decision
85 days
Submission Type
Summary