Last synced on 25 January 2026 at 3:41 am

NUVASIVE SPHERX SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K060225
510(k) Type
Special
Applicant
Nuvasive, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/12/2006
Days to Decision
72 days
Submission Type
Summary

NUVASIVE SPHERX SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K060225
510(k) Type
Special
Applicant
Nuvasive, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/12/2006
Days to Decision
72 days
Submission Type
Summary