Last synced on 30 May 2025 at 11:05 pm

ARTHREX BIO-COMPRESSION SCREW

Page Type
Cleared 510(K)
PDF
FDA Hosted 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
FDA Hosted 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