Palo Alto ™

FDA UDI

Class II (US FDA UDI)

by Cardinal Spine Llc

Identity

Trade Name: Palo Alto ™ FDA UDI
Generic Name: Vertebral body prosthesis, non-sterile FDA UDI
Device Name: CVBR LCM 23.25 MM FDA UDI
Model / Reference: LCM 23.25 MM FDA UDI
Description: CVBR LCM 23.25 MM FDA UDI

Identifiers

Catalog Number: LCM 23.25 MM FDA UDI
Primary DI / UDI-DI: 00852587007732 FDA UDI
FDA Product Code: PLR FDA UDI
GMDN Term: Vertebral body prosthesis, non-sterile 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

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size: Width — 13 Millimeter FDA UDI
Depth — 12 Millimeter FDA UDI
Height — 23.25 Millimeter FDA UDI

Category: Vertebral body prosthesis, non-sterile

Palo Alto ™ by Cardinal Spine Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Cardinal Spine Llc

Sources (1)

FDA UDI 3473709a-aac5-42fc-9e8e-87623de4c9e2 36 fields · synced May 30, 2026