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NUVASIVE CEMENT RESTRICTOR

Page Type
Cleared 510(K)
510(k) Number
K032180
510(k) Type
Traditional
Applicant
NUVASIVE, INC.
Country
United States
FDA Decision
Substantially Equivalent - With Limitations
Decision Date
10/7/2003
Days to Decision
82 days
Submission Type
Summary

NUVASIVE CEMENT RESTRICTOR

Page Type
Cleared 510(K)
510(k) Number
K032180
510(k) Type
Traditional
Applicant
NUVASIVE, INC.
Country
United States
FDA Decision
Substantially Equivalent - With Limitations
Decision Date
10/7/2003
Days to Decision
82 days
Submission Type
Summary