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Octane T

FDA UDI

Class I (US FDA UDI)

by Choicespine, LP

Identity

Trade Name
Octane T FDA UDI
Generic Name
Polymeric spinal interbody fusion cage FDA UDI
Device Name
OCTANE,SM AXL Z-CONN HANDLE FDA UDI
Model / Reference
600-9071 FDA UDI
Description
OCTANE,SM AXL Z-CONN HANDLE FDA UDI

Identifiers

Primary DI / UDI-DI
00840996155700 FDA UDI
510(k) Number
K070218 FDA UDI
FDA Product Code
LXH FDA UDI
GMDN Term
Polymeric spinal interbody fusion cage FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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: Polymeric spinal interbody fusion cage

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

Similar devices

Also classified as Polymeric spinal interbody fusion cage.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Choicespine, LP

Sources (1)

  • FDA UDI 56db9a36-e9b1-401a-abc6-53d6dc3120b6 34 fields · synced May 30, 2026