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4cis Peek Plif Cage System

FDA UDI

Class II (US FDA UDI)

by Alphanox Co., Ltd.

Identity

Trade Name
4CIS PEEK PLIF CAGE SYSTEM FDA UDI
Generic Name
Polymeric spinal interbody fusion cage FDA UDI
Device Name
4CIS® PEEK PLIF Cage 0 , 25x11x14mm FDA UDI
Model / Reference
5800-0014 FDA UDI
Description
4CIS® PEEK PLIF Cage 0 , 25x11x14mm FDA UDI

Identifiers

Catalog Number
5800-0014 FDA UDI
Primary DI / UDI-DI
08806373527081 FDA UDI
510(k) Number
K092162 FDA UDI
K190563 FDA UDI
FDA Product Code
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

No

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

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Polymeric spinal interbody fusion cage

4cis Peek Plif Cage System by Alphanox Co., Ltd. — 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

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Manufacturer

Manufacturer
Alphanox Co., Ltd.

Sources (1)

  • FDA UDI 433a8f9f-2d9a-4ef7-8f60-a5b5967500af 35 fields · synced Jun 8, 2026