Na 395.682
by Synthes United States GUDID
Product code LXT
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number10886982200518 | Date14 Sep 2015 | StatusIn distribution |
Coverage
- Listed
- Not covered
United States — GUDID listing Listed
Recalls
-
- Terminated Z-2451-2015
Labeling changes were made related to MR conditions that align with standard definitions for MR Safe, MR Conditional, and MR Unsafe. This recall identifies additional Trauma External Fixation System part numbers that should be considered MR Conditional. One serious injury reported.
-
- Terminated Z-1833-2014
Labeling changes have been made related to MR (Magnetic Resonance imaging) conditions as a result of changes in required protocols to designate a product MR Safe, MR Conditional, or MR Unsafe.
Specification
- Trade Name
- Na
- Generic Name
- External orthopaedic fixation system noninvasive component, single-use
- Model / Ref / Catalog
- 395.682, 395682
- Primary DI / UDI-DI
- 10886982200518
- FDA Product Code
- LXT, KTT
- GMDN Term
- External orthopaedic fixation system noninvasive component, single-use
- Device Class
- Class II
- Regulation Number
- 888.3030
- Commercial Distribution
- In Commercial Distribution
- Sterilization Method
- Moist Heat or Steam Sterilization
- MRI Safety
- MR Conditional
Other devices from Synthes
Properties & raw data
Show properties, registry sources and raw records
Other properties (11)
- Sterile: 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
- Manufacturing Date: No
Sources (1)
- FDA UDI c0735341-ac59-4da2-a619-4d08179408e9