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Octane Straight IR

FDA UDI

Class I (US FDA UDI)

by Choicespine, LP

Identity

Trade Name
Octane Straight IR FDA UDI
Generic Name
Polymeric spinal interbody fusion cage FDA UDI
Device Name
OCTANE STRAIGHT IR, Ti, 32X10X13, 6 DEG FDA UDI
Model / Reference
PT23-32136 FDA UDI
Description
OCTANE STRAIGHT IR, Ti, 32X10X13, 6 DEG FDA UDI

Identifiers

Primary DI / UDI-DI
00840996163781 FDA UDI
510(k) Number
K162103 FDA UDI
FDA Product Code
MPQ FDA UDI
MAX FDA UDI
GMDN Term
Polymeric spinal interbody fusion cage FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
864.3260 FDA UDI
888.3080 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
Length — 10 Millimeter FDA UDI
Width — 32 Millimeter FDA UDI
Height — 13 Millimeter FDA UDI

Category: Polymeric spinal interbody fusion cage

Octane Straight IR 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 d242b889-7642-41ca-8697-a0fd785a7cc5 36 fields · synced May 31, 2026