GSO GS1 Cannulated Screw System

FDA UDI

Class II (US FDA UDI)

by Unified Spine, Llc

Identity

Trade Name: GSO GS1 Cannulated Screw System FDA UDI
Generic Name: Spinal bone screw, non-bioabsorbable FDA UDI
Device Name: Notched Head Cannulated Multi-Axial Screw FDA UDI
Model / Reference: 508366 FDA UDI
Description: Notched Head Cannulated Multi-Axial Screw FDA UDI

Identifiers

Primary DI / UDI-DI: M9935083660 FDA UDI
FDA Product Code: MNI FDA UDI
MNH FDA UDI
KWP FDA UDI
GMDN Term: Spinal bone screw, non-bioabsorbable FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 888.3070 FDA UDI
888.3050 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Spinal bone screw, non-bioabsorbable

GSO GS1 Cannulated Screw System by Unified Spine, Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Also classified as Spinal bone screw, non-bioabsorbable.

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Unified Spine, Llc

Sources (1)

FDA UDI 71d483dd-0397-495a-9d64-eaa670068bae 34 fields · synced May 31, 2026