Last synced on 2 May 2025 at 11:05 pm

NUVASIVE BENDINI SPINAL ROD BENDING SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K122742
510(k) Type
Special
Applicant
NUVASIVE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/7/2012
Days to Decision
91 days
Submission Type
Summary

NUVASIVE BENDINI SPINAL ROD BENDING SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K122742
510(k) Type
Special
Applicant
NUVASIVE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/7/2012
Days to Decision
91 days
Submission Type
Summary