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NUVASIVE ANTERIOR LUMBAR PLATE SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K111866
510(k) Type
Special
Applicant
NUVASIVE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/22/2011
Days to Decision
22 days
Submission Type
Summary

NUVASIVE ANTERIOR LUMBAR PLATE SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K111866
510(k) Type
Special
Applicant
NUVASIVE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/22/2011
Days to Decision
22 days
Submission Type
Summary