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MODIFICATION TO PREFERENCE PEDICLE SCREW SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K081883
510(k) Type
Traditional
Applicant
US SPINE
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/24/2008
Days to Decision
84 days
Submission Type
Summary

MODIFICATION TO PREFERENCE PEDICLE SCREW SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K081883
510(k) Type
Traditional
Applicant
US SPINE
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/24/2008
Days to Decision
84 days
Submission Type
Summary