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GX Navigation Instrument System

Page Type
Cleared 510(K)
510(k) Number
K202836
510(k) Type
Traditional
Applicant
Life Spine Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/19/2021
Days to Decision
328 days
Submission Type
Summary

GX Navigation Instrument System

Page Type
Cleared 510(K)
510(k) Number
K202836
510(k) Type
Traditional
Applicant
Life Spine Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/19/2021
Days to Decision
328 days
Submission Type
Summary