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LAMINOPLASTY FIXATION SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K091623
510(k) Type
Traditional
Applicant
NUVASIVE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/9/2009
Days to Decision
128 days
Submission Type
Summary

LAMINOPLASTY FIXATION SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K091623
510(k) Type
Traditional
Applicant
NUVASIVE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/9/2009
Days to Decision
128 days
Submission Type
Summary