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BENDINI(TM) 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
K111811
510(k) Type
Traditional
Applicant
NUVASIVE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/5/2011
Days to Decision
161 days
Submission Type
Summary

BENDINI(TM) 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
K111811
510(k) Type
Traditional
Applicant
NUVASIVE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/5/2011
Days to Decision
161 days
Submission Type
Summary