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AOS CANNULATED BONE SCREW SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K014185
510(k) Type
Traditional
Applicant
ADVANCED ORTHOPAEDIC SOLUTIONS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/13/2002
Days to Decision
55 days
Submission Type
Summary

AOS CANNULATED BONE SCREW SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K014185
510(k) Type
Traditional
Applicant
ADVANCED ORTHOPAEDIC SOLUTIONS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/13/2002
Days to Decision
55 days
Submission Type
Summary