Identity
- Trade Name
- JOURNEY II XR FDA UDI
- Generic Name
- Orthopaedic bur, reusable FDA UDI
- Device Name
- JOURNEY II XR TIBIAL KEEL DRILL FDA UDI
- Model / Reference
- 74013993 FDA UDI
- Description
- JOURNEY II XR TIBIAL KEEL DRILL FDA UDI
Identifiers
- Catalog Number
- 74013993 FDA UDI
- Primary DI / UDI-DI
- 00885556696088 FDA UDI
- 510(k) Number
- K173331 FDA UDI
- FDA Product Code
- JWH FDA UDI
- GMDN Term
- Orthopaedic bur, reusable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3560 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 bur, reusable
Journey Ii Xr by Smith & Nephew, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Orthopaedic bur, reusable.
- KOMET Surgical Bur — Gebr. Brasseler GmbH & Co. KG · Class I
- KOMET Surgical Bur — Gebr. Brasseler GmbH & Co. KG · Class I
- Midas Rex Clearview™ — MEDTRONIC XOMED, INC. · Class II
- KOMET Surgical Bur — Gebr. Brasseler GmbH & Co. KG · Class I
- KOMET Surgical Bur — Gebr. Brasseler GmbH & Co. KG · Class I
- Uniglide Unicondylar Knee Prosthesis — CORIN LTD · Class II
- KOMET Surgical Bur — Gebr. Brasseler GmbH & Co. KG · Class I
- KOMET Surgical Bur — Gebr. Brasseler GmbH & Co. KG · Class I
Cleared under the same submission
K173331 also covers:
- JOURNEY II XR — Smith & Nephew, Inc.
- JOURNEY II XR — Smith & Nephew, Inc.
- JOURNEY II XR — Smith & Nephew, Inc.
- JOURNEY II XR — Smith & Nephew, Inc.
- JOURNEY II XR — Smith & Nephew, Inc.
- JOURNEY II XR — Smith & Nephew, Inc.
- JOURNEY II XR — Smith & Nephew, Inc.
- JOURNEY II XR — Smith & Nephew, Inc.
- JOURNEY II XR — Smith & Nephew, Inc.
- JOURNEY II XR — Smith & Nephew, Inc.
- JOURNEY II XR — Smith & Nephew, Inc.
- JOURNEY II XR — 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 |
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Manufacturer
- Manufacturer
- Smith & Nephew, Inc.
Sources (1)
- FDA UDI 0018acac-8607-4c8c-a491-8e58d46c4f85 36 fields · synced Jun 6, 2026