Last synced on 14 November 2025 at 11:06 pm

NUVASIVE HELIX-T ACP SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K083341
510(k) Type
Special
Applicant
NUVASIVE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/20/2009
Days to Decision
128 days
Submission Type
Summary

NUVASIVE HELIX-T ACP SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K083341
510(k) Type
Special
Applicant
NUVASIVE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/20/2009
Days to Decision
128 days
Submission Type
Summary