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Channel Cervical

FDA UDI

Class II (US FDA UDI)

by Pantheon Spinal LLC

Identity

Trade Name
Channel Cervical FDA UDI
Generic Name
Polymeric spinal interbody fusion cage FDA UDI
Device Name
Spacer Cervical 9mm x 6 deg PEEK FDA UDI
Model / Reference
1 FDA UDI
Description
Spacer Cervical 9mm x 6 deg PEEK FDA UDI

Identifiers

Catalog Number
C091412-6 FDA UDI
Primary DI / UDI-DI
B528C09141260 FDA UDI
FDA Product Code
ODP FDA UDI
GMDN Term
Polymeric spinal interbody fusion cage 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

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: Polymeric spinal interbody fusion cage

Channel Cervical by Pantheon Spinal LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Polymeric spinal interbody fusion cage.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Pantheon Spinal LLC

Sources (1)

  • FDA UDI 9493cfd3-2dba-410a-b4e5-38e1f708a072 35 fields · synced May 30, 2026