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PressON Spinal Fixation System

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K223529
510(k) Type
Traditional
Applicant
Nexus Spine, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/2/2023
Days to Decision
160 days
Submission Type
Summary

PressON Spinal Fixation System

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K223529
510(k) Type
Traditional
Applicant
Nexus Spine, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/2/2023
Days to Decision
160 days
Submission Type
Summary