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PressON Pro Spinal Fixation System

Page Type
Cleared 510(K)
510(k) Number
K160820
510(k) Type
Traditional
Applicant
Nexus Spine, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/28/2016
Days to Decision
96 days
Submission Type
Summary

PressON Pro Spinal Fixation System

Page Type
Cleared 510(K)
510(k) Number
K160820
510(k) Type
Traditional
Applicant
Nexus Spine, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/28/2016
Days to Decision
96 days
Submission Type
Summary