Identity
- Trade Name
- Contour FDA UDI
- Generic Name
- Acetabulum prosthesis trial, prefabricated, reusable FDA UDI
- Device Name
- CONTOUR RECONSTRUCTION RING TRIAL 56MM OUTER DIAMTER 52MM INNER DIAMETER LEFT FDA UDI
- Model / Reference
- 71367156 FDA UDI
- Description
- CONTOUR RECONSTRUCTION RING TRIAL 56MM OUTER DIAMTER 52MM INNER DIAMETER LEFT FDA UDI
Identifiers
- Catalog Number
- 71367156 FDA UDI
- Primary DI / UDI-DI
- 03596010451842 FDA UDI
- 510(k) Number
- K123598 FDA UDI
- FDA Product Code
- JDG FDA UDI
- GMDN Term
- Acetabulum prosthesis trial, prefabricated, reusable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3360 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
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
Category: Acetabulum prosthesis trial, prefabricated, reusable
Contour by Smith & Nephew, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Acetabulum prosthesis trial, prefabricated, reusable.
- Trabecular Metal® — Zimmer, Inc. · Class I
- G7 PROVISIONAL SHELL — Biomet Orthopedics, Inc. · Class II
- Bipolar Head — Limacorporate · Class II
- Acetabular Cups — Limacorporate · Class II
- Novation — Exactech, Inc. · Class I
- TRIAL NECK for Exacta S Rasp - Mark S - Standard — Permedica S.p.A · Class IIa
- INSTRUMENT — Howmedica Osteonics Corp. · Class II
- MultiPolar® — Zimmer, Inc. · Class I
Cleared under the same submission
K123598 also covers:
- 'SL-PLUS¿' — Smith & Nephew, Inc.
- ANTHOLOGY — Smith & Nephew, Inc.
- ANTHOLOGY — Smith & Nephew, Inc.
- Accord — Smith & Nephew, Inc.
- Anthology — Smith & Nephew, Inc.
- Anthology — Smith & Nephew, Inc.
- Anthology — Smith & Nephew, Inc.
- Anthology — Smith & Nephew, Inc.
- Anthology — Smith & Nephew, Inc.
- Anthology — Smith & Nephew, Inc.
- CATALYSTEM — 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 1d64dbbe-eb1b-4ed9-a09c-b37fd631e013 36 fields · synced Jun 8, 2026