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FDA 510(k) K231850, QUARTEX® Occipito-Cervico-Thoracic Spinal System ExcelsiusGPS® Instruments, Globus Medical Inc
FDA 510(k) K231850, QUARTEX® Occipito-Cervico-Thoracic Spinal System ExcelsiusGPS® Instruments, Globus Medical Inc
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$49.00 USD
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$49.00 USD
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510(K) Number: K231850
Device Name: QUARTEX® Occipito-Cervico-Thoracic Spinal System ExcelsiusGPS® Instruments
Manufacturer: Globus Medical Inc
Device Classification Name: Posterior Cervical Screw System
Regulation Number: 888.3075
Classification Product Code: NKG
Date Received: 06/23/2023
Decision Date: 03/14/2024
Regulation Medical Specialty: Orthopedic
Device Name: QUARTEX® Occipito-Cervico-Thoracic Spinal System ExcelsiusGPS® Instruments
Manufacturer: Globus Medical Inc
Device Classification Name: Posterior Cervical Screw System
Regulation Number: 888.3075
Classification Product Code: NKG
Date Received: 06/23/2023
Decision Date: 03/14/2024
Regulation Medical Specialty: Orthopedic
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