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NUVASIVE LONG LATERAL SPINAL SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K122081
510(k) Type
Special
Applicant
NUVASIVE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/1/2013
Days to Decision
200 days
Submission Type
Summary

NUVASIVE LONG LATERAL SPINAL SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K122081
510(k) Type
Special
Applicant
NUVASIVE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/1/2013
Days to Decision
200 days
Submission Type
Summary