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Evolution®

FDA UDI

Class II (US FDA UDI)

by MicroPort Orthopedics Inc.

Identity

Trade Name
EVOLUTION® FDA UDI
Generic Name
Knee femur stem prosthesis FDA UDI
Model / Reference
ESP23150 FDA UDI

Identifiers

Catalog Number
ESP23150 FDA UDI
Primary DI / UDI-DI
M684ESP231501 FDA UDI
FDA Product Code
JWH FDA UDI
GMDN Term
Knee femur stem prosthesis FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3560 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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size
Length — 150 Millimeter FDA UDI
Outer Diameter — 23 Millimeter FDA UDI

Category: Knee femur stem prosthesis

Evolution® by MicroPort Orthopedics Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Knee femur stem prosthesis.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 982ed870-18fb-4a6b-8b80-4f1e63709b55 35 fields · synced Jun 9, 2026