← Back to catalogue

Valeo Ii

FDA UDI

Class II (US FDA UDI)

by CTL Medical Corporation

Identity

Trade Name
VALEO II FDA UDI
Generic Name
Polymeric spinal interbody fusion cage FDA UDI
Device Name
Valeo II LL 18x40x08mm, 6deg FDA UDI
Model / Reference
11.020.3408 FDA UDI
Description
Valeo II LL 18x40x08mm, 6deg FDA UDI

Identifiers

Primary DI / UDI-DI
00841732158054 FDA UDI
510(k) Number
K121892 FDA UDI
FDA Product Code
ODP FDA UDI
MAX 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

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Polymeric spinal interbody fusion cage

Valeo Ii by CTL Medical Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Polymeric spinal interbody fusion cage.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI a8638288-9eb8-4f97-b6d9-7ed14695e26a 34 fields · synced May 30, 2026