Octane Straight

FDA UDI

Class II (US FDA UDI)

by Choicespine, LP

Identity

Trade Name: Octane Straight FDA UDI
Generic Name: Polymeric spinal fusion cage, sterile FDA UDI
Model / Reference: 05-071-01-2809 FDA UDI

Identifiers

Catalog Number: 05-071-01-2809 FDA UDI
Primary DI / UDI-DI: 10885862235855 FDA UDI
FDA Product Code: MAX FDA UDI
GMDN Term: Polymeric spinal fusion cage, sterile FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 888.3080 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

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

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Dimensions & Sizes

Size: Width — 28 Millimeter FDA UDI
Length — 10 Millimeter FDA UDI
Height — 9 Millimeter FDA UDI

Category: Polymeric spinal fusion cage, sterile

Octane Straight by Choicespine, LP — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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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: Choicespine, LP

Sources (1)

FDA UDI 2e29a90c-62bb-4cd1-95d5-a2442cca75b7 34 fields · synced May 30, 2026