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QUARTEX Occipito-Cervico-Thoracic Spinal System, Globus Navigation Instruments

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K211957
510(k) Type
Traditional
Applicant
Globus Medical Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/18/2021
Days to Decision
55 days
Submission Type
Summary

QUARTEX Occipito-Cervico-Thoracic Spinal System, Globus Navigation Instruments

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K211957
510(k) Type
Traditional
Applicant
Globus Medical Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/18/2021
Days to Decision
55 days
Submission Type
Summary