Identity
- Trade Name
- JOURNEY FDA UDI
- Generic Name
- Orthopaedic reamer guide FDA UDI
- Device Name
- JOURNEY II UK RESECTION ANTERIOR/POSTERIOR BLOCK RIGHT MEDIAL/LEFT LATERAL SZ 8 FDA UDI
- Model / Reference
- 74016418 FDA UDI
- Description
- JOURNEY II UK RESECTION ANTERIOR/POSTERIOR BLOCK RIGHT MEDIAL/LEFT LATERAL SZ 8 FDA UDI
Identifiers
- Catalog Number
- 74016418 FDA UDI
- Primary DI / UDI-DI
- 00885556690093 FDA UDI
- 510(k) Number
- K190085 FDA UDI
- FDA Product Code
- HSX FDA UDI
- GMDN Term
- Orthopaedic reamer guide FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3520 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
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
No
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Orthopaedic reamer guide
Journey by Smith & Nephew, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Orthopaedic reamer guide.
- Revision Knee System — SHALBY ADVANCED TECHNOLOGIES, INC. · Class I
- Cone Reamer Guide — TOTAL JOINT ORTHOPEDICS, INC. · Class I
- SMR Shoulder — Limacorporate · Class II
- PRIMA TT Glenoid — Limacorporate · Class II
- MAXIM RESECTION DISTAL — Biomet Orthopedics, Inc. · Class I
- Arthrex® — Arthrex, Inc. · Class I
- VANGUARD XP — Biomet Orthopedics, Inc. · Class I
- MAXIM EM TIBIAL GUIDE — Biomet Orthopedics, Inc. · Class I
Cleared under the same submission
K190085 also covers:
- JOURNEY — Smith & Nephew, Inc.
- JOURNEY — Smith & Nephew, Inc.
- JOURNEY — Smith & Nephew, Inc.
- JOURNEY — Smith & Nephew, Inc.
- JOURNEY — Smith & Nephew, Inc.
- JOURNEY — Smith & Nephew, Inc.
- JOURNEY — Smith & Nephew, Inc.
- JOURNEY — Smith & Nephew, Inc.
- JOURNEY — Smith & Nephew, Inc.
- JOURNEY — Smith & Nephew, Inc.
- JOURNEY — Smith & Nephew, Inc.
- JOURNEY — 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 98f9c57c-027c-4ac5-b68a-64247a4b0942 36 fields · synced Jun 8, 2026