U-Motion II™ 1203-6632-RA
Listed
Valid until
Not applicable
FDA recalls
None foundDocuments
None
Trust
Unverified
Overview
Improve your femoral head prosthesis trial with the U-Motion II ceramic femoral head, a cutting-edge device designed for orthopedic surgeons to assess and adjust the correct fit of final prostheses. This reusable device features a unique ceramic design, multiple trial sizes, and adjustable adapters. By using the U-Motion II, you can achieve optimal offset, leg-length, and range of motion, ultimately leading to better patient outcomes.
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number04719872160069 | Date18 May 2017 | StatusListed |
Recalls
No FDA recalls found in the data synced 23 Oct 2026.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade Name
- U-Motion II™
- Generic Name
- Femoral head prosthesis trial
- Model / Ref / Catalog
- 1203-6632-RA
- Primary DI / UDI-DI
- 04719872160069
- 510(k) Number
- FDA Product Code
- LWJ, MEH, LPH
- GMDN Term
- Femoral head prosthesis trial
- Device Class
- Class II
- Regulation Number
- 888.3360, 888.3353, 888.3358
- GUDID distribution status
- In Commercial Distribution
- Sterilization Method
- Moist Heat or Steam Sterilization
Other devices from United Orthopedic Corp.
Properties
Other properties (11)
- Sterile: No
- Single Use: No
- Implantable: No
- Contains Latex: No
- Over-the-Counter: No
- Convenience Kit: No
- Combination Product: No
- HCT/P: No
- Premarket Exempt: No
- Serial Number: No
- Expiration Date: No