Last synced on 13 June 2025 at 11:06 pm

Palladian Lumbar Pedicle Screw System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K143230
510(k) Type
Traditional
Applicant
Neurostructures, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/25/2015
Days to Decision
107 days
Submission Type
Summary

Palladian Lumbar Pedicle Screw System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K143230
510(k) Type
Traditional
Applicant
Neurostructures, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/25/2015
Days to Decision
107 days
Submission Type
Summary