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NUVASIVE HELIX ACP SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K071329
510(k) Type
Special
Applicant
NUVASIVE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/8/2007
Days to Decision
89 days
Submission Type
Summary

NUVASIVE HELIX ACP SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K071329
510(k) Type
Special
Applicant
NUVASIVE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/8/2007
Days to Decision
89 days
Submission Type
Summary