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ARCUATE VERTEBRAL AUGMENTATION SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K063248
510(k) Type
Traditional
Applicant
MEDTRONIC SOFAMOR DANEK
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/13/2007
Days to Decision
138 days
Submission Type
Summary

ARCUATE VERTEBRAL AUGMENTATION SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K063248
510(k) Type
Traditional
Applicant
MEDTRONIC SOFAMOR DANEK
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/13/2007
Days to Decision
138 days
Submission Type
Summary