Identity
- Trade Name
- Contour FDA UDI
- Generic Name
- Metallic acetabulum prosthesis FDA UDI
- Device Name
- CONTOUR ACETABULAR RECONSTRUCTION RING 62MM OUTER DIAMETER 58MM INNER DIAMETER RIGHT FDA UDI
- Model / Reference
- 71337262 FDA UDI
- Description
- CONTOUR ACETABULAR RECONSTRUCTION RING 62MM OUTER DIAMETER 58MM INNER DIAMETER RIGHT FDA UDI
Identifiers
- Catalog Number
- 71337262 FDA UDI
- Primary DI / UDI-DI
- 03596010293343 FDA UDI
- FDA Product Code
- JDJ FDA UDI
- GMDN Term
- Metallic acetabulum prosthesis FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 878.3300 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
MR Conditional FDA UDI
Category: Metallic acetabulum prosthesis
Contour by Smith & Nephew, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Metallic acetabulum prosthesis.
- TRABECULAR METAL™ — Zimmer Trabecular Metal Technology, Inc. · Class II
- Lineage — MicroPort Orthopedics Inc. · Class II
- Lineage — MicroPort Orthopedics Inc. · Class II
- Dynasty — MicroPort Orthopedics Inc. · Class II
- Platform Acetabular Cup with Ti-Coat — TOTAL JOINT ORTHOPEDICS, INC. · Class II
- PRIME — MicroPort Orthopedics Inc. · Class II
- PROCOTYL® PRIME — MicroPort Orthopedics Inc. · Class II
- Lineage — MicroPort Orthopedics Inc. · Class II
Cleared under the same submission
K211176 also covers:
- BUCK — Smith & Nephew, Inc.
- Conquest FX — Smith & Nephew, Inc.
- ECHELON — Smith & Nephew, Inc.
- ECHELON — Smith & Nephew, Inc.
- ECHELON — Smith & Nephew, Inc.
- ECHELON — Smith & Nephew, Inc.
- POLARCUP — Smith & Nephew, Inc.
- POLARCUP — Smith & Nephew, Inc.
- POLARCUP — Smith & Nephew, Inc.
- POLARCUP — Smith & Nephew, Inc.
- POLARCUP — Smith & Nephew, Inc.
- R3 — Smith & Nephew, Inc.
K962541 also covers:
- Contour — Smith & Nephew, Inc.
- Contour — Smith & Nephew, Inc.
- Contour — Smith & Nephew, Inc.
- Contour — Smith & Nephew, Inc.
- Contour — Smith & Nephew, Inc.
- Contour — Smith & Nephew, Inc.
- Contour — Smith & Nephew, Inc.
- Contour — Smith & Nephew, Inc.
- Contour — Smith & Nephew, Inc.
- Contour — Smith & Nephew, Inc.
- Contour — Smith & Nephew, Inc.
- Contour — 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 4ffc5944-0262-4a1e-a9e2-2fee82688dd9 37 fields · synced Jun 8, 2026