Last synced on 14 November 2025 at 11:06 pm

Augment Off-Axis Instrument System

Page Type
Cleared 510(K)
510(k) Number
K241043
510(k) Type
Special
Applicant
Fix Surgical
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/15/2024
Days to Decision
28 days
Submission Type
Summary

Augment Off-Axis Instrument System

Page Type
Cleared 510(K)
510(k) Number
K241043
510(k) Type
Special
Applicant
Fix Surgical
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/15/2024
Days to Decision
28 days
Submission Type
Summary