Identity
- Trade Name
- EVOS FDA UDI
- Generic Name
- Orthopaedic bone screw (non-sliding) FDA UDI
- Device Name
- EVOS 3.5MM X 10MM CORTEX SCREW SELF-TAPPING FDA UDI
- Model / Reference
- 72403510N FDA UDI
- Description
- EVOS 3.5MM X 10MM CORTEX SCREW SELF-TAPPING FDA UDI
Identifiers
- Catalog Number
- 72403510N FDA UDI
- Primary DI / UDI-DI
- 00885556637920 FDA UDI
- FDA Product Code
- HWC FDA UDIHRS FDA UDI
- GMDN Term
- Orthopaedic bone screw (non-sliding) FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3040 FDA UDI888.3030 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
Moist Heat or Steam Sterilization FDA UDI
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).
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- Zavation — ZAVATION · Class II
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- Arthrex® — Arthrex, Inc. · Class II
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- PANGEA — Stryker Corp. · Class II
- ARIX System Bone Screw — Jeil Medical Corporation · Class II
Cleared under the same submission
K162078 also covers:
- EVOS — Smith & Nephew, Inc.
- EVOS — Smith & Nephew, Inc.
- EVOS — Smith & Nephew, Inc.
- EVOS — Smith & Nephew, Inc.
- EVOS — Smith & Nephew, Inc.
- EVOS — Smith & Nephew, Inc.
- EVOS — Smith & Nephew, Inc.
- EVOS — Smith & Nephew, Inc.
- EVOS — Smith & Nephew, Inc.
- EVOS — Smith & Nephew, Inc.
- EVOS — Smith & Nephew, Inc.
- EVOS — Smith & Nephew, Inc.
K172262 also covers:
- EVOS — Smith & Nephew, Inc.
- EVOS — Smith & Nephew, Inc.
- EVOS — Smith & Nephew, Inc.
- EVOS — Smith & Nephew, Inc.
- EVOS — Smith & Nephew, Inc.
- EVOS — Smith & Nephew, Inc.
- EVOS — Smith & Nephew, Inc.
- EVOS — Smith & Nephew, Inc.
- EVOS — Smith & Nephew, Inc.
- EVOS — Smith & Nephew, Inc.
- EVOS — Smith & Nephew, Inc.
- EVOS — Smith & Nephew, Inc.
K210837 also covers:
- CHS — Smith & Nephew, Inc.
- CHS — Smith & Nephew, Inc.
- D-RAD SMART PACK — Smith & Nephew, Inc.
- EVOS — Smith & Nephew, Inc.
- EVOS — Smith & Nephew, Inc.
- EVOS — Smith & Nephew, Inc.
- EVOS — Smith & Nephew, Inc.
- EVOS — Smith & Nephew, Inc.
- EVOS — Smith & Nephew, Inc.
- EVOS — Smith & Nephew, Inc.
- EVOS — Smith & Nephew, Inc.
- EVOS — Smith & Nephew, Inc.
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Smith & Nephew, Inc.
Sources (1)
- FDA UDI 1e260fe0-18c6-4120-aaf8-39b85bb25323 36 fields · synced Jun 8, 2026