Last synced on 14 November 2025 at 11:06 pm

Caliber Intramedullary Fixation System

Page Type
Cleared 510(K)
510(k) Number
K242896
510(k) Type
Traditional
Applicant
Nvision Biomedical Technologies
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/5/2025
Days to Decision
135 days
Submission Type
Summary

Caliber Intramedullary Fixation System

Page Type
Cleared 510(K)
510(k) Number
K242896
510(k) Type
Traditional
Applicant
Nvision Biomedical Technologies
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/5/2025
Days to Decision
135 days
Submission Type
Summary