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Octane T

FDA UDI

Class II (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 T,NON-STRL 11MM FDA UDI
Model / Reference
600-1111 FDA UDI
Description
OCTANE T,NON-STRL 11MM FDA UDI

Identifiers

Primary DI / UDI-DI
00840996169141 FDA UDI
510(k) Number
K070218 FDA UDI
FDA Product Code
MQP FDA UDI
GMDN Term
Polymeric spinal interbody fusion cage FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3060 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

Dimensions & Sizes

Size
Width — 10 Millimeter FDA UDI
Length — 27 Millimeter FDA UDI
Height — 11 Millimeter FDA UDI

Category: Polymeric spinal interbody fusion cage

Octane T by Choicespine, LP — Class II — 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 b59ec2a8-2558-4886-bb8c-06e4218fce0a 36 fields · synced Jun 6, 2026