Last synced on 9 May 2025 at 11:05 pm

NUVASIVE ADJUSTABLE VERTEBRAL BODY REPLACEMENT SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K090176
510(k) Type
Special
Applicant
NUVASIVE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/27/2009
Days to Decision
94 days
Submission Type
Summary

NUVASIVE ADJUSTABLE VERTEBRAL BODY REPLACEMENT SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K090176
510(k) Type
Special
Applicant
NUVASIVE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/27/2009
Days to Decision
94 days
Submission Type
Summary