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ARS SCREW; SLANT SCREW

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K130954
510(k) Type
Traditional
Applicant
Advanced Interventional Technology, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/31/2013
Days to Decision
56 days
Submission Type
Summary

ARS SCREW; SLANT SCREW

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K130954
510(k) Type
Traditional
Applicant
Advanced Interventional Technology, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/31/2013
Days to Decision
56 days
Submission Type
Summary