Last synced on 14 November 2025 at 11:06 pm

NuVasive® Precept™ Spinal System

Page Type
Cleared 510(K)
510(k) Number
K171894
510(k) Type
Traditional
Applicant
Nu Vasive, Incorporated
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/28/2017
Days to Decision
94 days
Submission Type
Summary

NuVasive® Precept™ Spinal System

Page Type
Cleared 510(K)
510(k) Number
K171894
510(k) Type
Traditional
Applicant
Nu Vasive, Incorporated
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/28/2017
Days to Decision
94 days
Submission Type
Summary