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Calix Spinal Implant System

FDA UDI

Class I (US FDA UDI)

by Xtant Medical Holdings, Inc.

Identity

Trade Name
Calix Spinal Implant System FDA UDI
Generic Name
Polymeric spinal interbody fusion cage FDA UDI
Device Name
SPECIALTY ROTATING TLIF INSERTER ASSEMBLY FDA UDI
Model / Reference
C034-0245 FDA UDI
Description
SPECIALTY ROTATING TLIF INSERTER ASSEMBLY FDA UDI

Identifiers

Primary DI / UDI-DI
M697C03402451 FDA UDI
FDA Product Code
HWA 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

Yes

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

Calix Spinal Implant System by Xtant Medical Holdings, Inc. — Class I — 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

Sources (1)

  • FDA UDI e9900d18-4bb2-43bb-bc2c-d15e47d79dc1 34 fields · synced May 31, 2026