Last synced on 2 May 2025 at 11:05 pm

Spine Navigation System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K233725
510(k) Type
Traditional
Applicant
Medivis, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/26/2024
Days to Decision
248 days
Submission Type
Summary

Spine Navigation System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K233725
510(k) Type
Traditional
Applicant
Medivis, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/26/2024
Days to Decision
248 days
Submission Type
Summary