Identity
- Trade Name
- ANTHOLOGY FDA UDI
- Generic Name
- Coated femoral stem prosthesis, modular FDA UDI
- Device Name
- ANTHOLOGY STANDARD OFFSET POROUS PLUS HYDROXYAPATITE SIZE 7 FDA UDI
- Model / Reference
- 71357007 FDA UDI
- Description
- ANTHOLOGY STANDARD OFFSET POROUS PLUS HYDROXYAPATITE SIZE 7 FDA UDI
Identifiers
- Catalog Number
- 71357007 FDA UDI
- Primary DI / UDI-DI
- 03596010559500 FDA UDI
- FDA Product Code
- MRA FDA UDIJDI FDA UDI
- GMDN Term
- Coated femoral stem prosthesis, modular FDA UDI
Classification
- Device Class
- Class III FDA UDI
- Regulation Number
- 888.3350 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
No
FDA UDI
MR Conditional FDA UDI
Category: Coated hip femur prosthesis, modularCoated femoral stem prosthesis, modular
Anthology by Smith & Nephew, Inc. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Coated femoral stem prosthesis, modular.
- MALLORY/HEAD CALCAR HIP SYSTEM — Biomet Orthopedics, Inc. · Class II
- TheRay Collared and Collarless Femoral Stem — Nextstep Arthropedix · Class II
- STERIZO Total Hip System — CPM Medical Consultants, LLC · Class II
- PROFEMUR® — MicroPort Orthopedics Inc. · Class II
- MALLORY/HEAD CALCAR HIP SYSTEM — Biomet Orthopedics, Inc. · Class II
- Alteon — Exactech, Inc. · Class II
- TheRay Collared and Collarless Femoral Stem — Nextstep Arthropedix · Class II
- Origin DAA Stem, Coxa Vara — SIGNATURE ORTHOPAEDICS PTY LTD · Class II
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 III | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Smith & Nephew, Inc.
Sources (1)
- FDA UDI 3d080bd5-5064-4aac-8615-a888acfc77b3 35 fields · synced Jun 8, 2026