Last synced on 25 April 2025 at 11:05 pm

Reline System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K142499
510(k) Type
Traditional
Applicant
NUVASIVE, INCORPORATED
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/19/2014
Days to Decision
75 days
Submission Type
Summary

Reline System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K142499
510(k) Type
Traditional
Applicant
NUVASIVE, INCORPORATED
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/19/2014
Days to Decision
75 days
Submission Type
Summary