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Medussa-PL Cage

FDA UDI

Class II (US FDA UDI)

by Medyssey Co., Ltd.

Identity

Trade Name
Medussa-PL Cage FDA UDI
Generic Name
Metallic spinal interbody fusion cage FDA UDI
Device Name
Non-sterile type, Medussa Cage, Medussa-PL Solid Type, (Angle)4°, (L)25mm, (H)8mm, (W)9mm FDA UDI
Model / Reference
MM42508A FDA UDI
Description
Non-sterile type, Medussa Cage, Medussa-PL Solid Type, (Angle)4°, (L)25mm, (H)8mm, (W)9mm FDA UDI

Identifiers

Primary DI / UDI-DI
08800048434919 FDA UDI
510(k) Number
K200283 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

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: Metallic spinal interbody fusion cage

Medussa-PL Cage by Medyssey Co., Ltd. — 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

Manufacturer
Medyssey Co., Ltd.

Sources (1)

  • FDA UDI 3ae53687-a8da-4c15-90fc-07c58508ee7a 34 fields · synced May 31, 2026