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RODIN Expandable Lumbar Cage System

FDA UDI

Class II (US FDA UDI)

by CTL Medical Corporation

Identity

Trade Name
RODIN Expandable Lumbar Cage System FDA UDI
Generic Name
General internal orthopaedic fixation system implantation kit FDA UDI
Device Name
RODIN Expansion Tamp FDA UDI
Model / Reference
027.7502 FDA UDI
Description
RODIN Expansion Tamp FDA UDI

Identifiers

Catalog Number
027.7502 FDA UDI
Primary DI / UDI-DI
00841732135307 FDA UDI
FDA Product Code
MQP FDA UDI
MAX FDA UDI
GMDN Term
General internal orthopaedic fixation system implantation kit FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3060 FDA UDI
888.3080 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

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

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: General internal orthopaedic fixation system implantation kit

RODIN Expandable Lumbar Cage System by CTL Medical Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General internal orthopaedic fixation system implantation kit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
CTL Medical Corporation

Sources (1)

  • FDA UDI f0a266e1-c1d0-419a-a8c5-7274b32ec17c 35 fields · synced May 30, 2026