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Precision Spine Navigation Instrumentation

Page Type
Cleared 510(K)
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)
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