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GRAFT CONTAINMENT DEVICE

Page Type
Cleared 510(K)
510(k) Number
K070148
510(k) Type
Traditional
Applicant
NUVASIVE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/31/2007
Days to Decision
196 days
Submission Type
Summary

GRAFT CONTAINMENT DEVICE

Page Type
Cleared 510(K)
510(k) Number
K070148
510(k) Type
Traditional
Applicant
NUVASIVE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/31/2007
Days to Decision
196 days
Submission Type
Summary