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Varian Cage

FDA UDI

Class II (US FDA UDI)

by Medyssey Co., Ltd.

Identity

Trade Name
Varian Cage FDA UDI
Generic Name
Polymeric spinal interbody fusion cage FDA UDI
Device Name
Varian Cage, Block Type Cage, (Height)12mm, (Expanding HeightL)15mm, (Width)11mm, (Length)24mm FDA UDI
Model / Reference
VB-1215M FDA UDI
Description
Varian Cage, Block Type Cage, (Height)12mm, (Expanding HeightL)15mm, (Width)11mm, (Length)24mm FDA UDI

Identifiers

Primary DI / UDI-DI
08809547368435 FDA UDI
510(k) Number
K172756 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

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Polymeric spinal interbody fusion cage

Varian Cage by Medyssey 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
Medyssey Co., Ltd.

Sources (1)

  • FDA UDI 7704a4b8-ddeb-48d0-8415-2f43e12dc37c 34 fields · synced Jun 8, 2026