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PARALLAX CONTOUR VERTEBRAL AUGMENTATION DEVICE

Page Type
Cleared 510(K)
510(k) Number
K100479
510(k) Type
Traditional
Applicant
Arthrocare Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/21/2010
Days to Decision
215 days
Submission Type
Summary

PARALLAX CONTOUR VERTEBRAL AUGMENTATION DEVICE

Page Type
Cleared 510(K)
510(k) Number
K100479
510(k) Type
Traditional
Applicant
Arthrocare Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/21/2010
Days to Decision
215 days
Submission Type
Summary