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IB3D™ PL Spinal System

FDA UDI

Class II (US FDA UDI)

by Medicrea International SA

Identity

Trade Name
IB3D™ PL Spinal System FDA UDI
Generic Name
Metallic spinal interbody fusion cage FDA UDI
Device Name
CAGE B241C13062209 3D PL 13X6DGX22X9MM FDA UDI
Model / Reference
B241C13062209 FDA UDI
Description
CAGE B241C13062209 3D PL 13X6DGX22X9MM FDA UDI

Identifiers

Primary DI / UDI-DI
03613720286257 FDA UDI
510(k) Number
K241164 FDA UDI
FDA Product Code
MAX FDA UDI
GMDN Term
Metallic 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

Yes

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
MRI Safety
MR Conditional FDA UDI

Category: Metallic spinal interbody fusion cage

IB3D™ PL Spinal System by Medicrea International SA — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Metallic 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

Sources (1)

  • FDA UDI 5c739762-cc0c-4443-91a2-a1f733e769c6 35 fields · synced May 31, 2026