Last synced on 14 November 2025 at 11:06 pm

FOCUS Pedicle Screw System

Page Type
Cleared 510(K)
510(k) Number
K180458
510(k) Type
Traditional
Applicant
Nvision Biomedical Technologies, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/17/2018
Days to Decision
56 days
Submission Type
Summary

FOCUS Pedicle Screw System

Page Type
Cleared 510(K)
510(k) Number
K180458
510(k) Type
Traditional
Applicant
Nvision Biomedical Technologies, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/17/2018
Days to Decision
56 days
Submission Type
Summary