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Evos

FDA UDI

Class II (US FDA UDI)

by Smith & Nephew, Inc.

Identity

Trade Name
EVOS FDA UDI
Generic Name
Orthopaedic bone screw (non-sliding) FDA UDI
Device Name
EVOS 2.7MM X 7MM CORTEX SCREW T8 SELF-TAPPING FDA UDI
Model / Reference
72402707N FDA UDI
Description
EVOS 2.7MM X 7MM CORTEX SCREW T8 SELF-TAPPING FDA UDI

Identifiers

Catalog Number
72402707N FDA UDI
Primary DI / UDI-DI
00885556449448 FDA UDI
510(k) Number
K140814 FDA UDI
K210837 FDA UDI
K213126 FDA UDI
FDA Product Code
HRS FDA UDI
GMDN Term
Orthopaedic bone screw (non-sliding) FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3030 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

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI
MRI Safety
MR Conditional FDA UDI

Category: Orthopaedic bone screw (non-sliding)

Evos by Smith & Nephew, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic bone screw (non-sliding).

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 748f0f72-e9fc-4399-a12e-e9b34c11dcb4 37 fields · synced Jun 8, 2026