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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
Bone-screw internal spinal fixation system rod FDA UDI
Device Name
Pre-Bent, Pointed Spinal Rod FDA UDI
Model / Reference
508290 FDA UDI
Description
Pre-Bent, Pointed Spinal Rod FDA UDI

Identifiers

Primary DI / UDI-DI
M9935082900 FDA UDI
FDA Product Code
KWP FDA UDI
MNH FDA UDI
MNI FDA UDI
GMDN Term
Bone-screw internal spinal fixation system rod FDA UDI

Classification

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

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Bone-screw internal spinal fixation system rod

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

Similar devices

Also classified as Bone-screw internal spinal fixation system rod.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Unified Spine, Llc

Sources (1)

  • FDA UDI 9b0c6f57-d482-4baa-9ab3-0e1c9ee73dcc 34 fields · synced Jun 6, 2026