Last synced on 18 April 2025 at 11:05 pm

ONX Large External Fixation System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K213905
510(k) Type
Traditional
Applicant
OrthoNovis, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/25/2022
Days to Decision
254 days
Submission Type
Summary

ONX Large External Fixation System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K213905
510(k) Type
Traditional
Applicant
OrthoNovis, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/25/2022
Days to Decision
254 days
Submission Type
Summary