Last synced on 2 May 2025 at 11:05 pm

Precision Spine Navigation Instrumentation

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K181606
510(k) Type
Traditional
Applicant
Precision Spine, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/27/2019
Days to Decision
465 days
Submission Type
Summary

Precision Spine Navigation Instrumentation

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K181606
510(k) Type
Traditional
Applicant
Precision Spine, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/27/2019
Days to Decision
465 days
Submission Type
Summary