Simplify® Cervical Artificial Disc
Listed
Valid until
Not applicable
FDA recalls
1 ongoingDocuments
None
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00843285100733 | Date14 Dec 2020 | StatusListed |
Recalls
-
- Ongoing Z-1453-2022
Cervical artificial disc Unique Device Identifier (UDI) barcodes contain the incorrect Global Trade Item Number (GTIN) on the Patient Label when scanned and may also contain the incorrect GTIN human readable text, which could lead to selecting an incorrectly sized unit.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Generic Name
- Spinal implant trial
- Model / Ref / Catalog
- E, T-MD-6L
- Description
- Simplify® Trial, Size MD, Height 6, 5° Lordosis
- Primary DI / UDI-DI
- 00843285100733
- PMA Number
- FDA Product Code
- MJO
- GMDN Term
- Spinal implant trial
- Device Class
- Class III
- GUDID distribution status
- In Commercial Distribution
- Sterilization Method
- Moist Heat or Steam Sterilization
- Size
- Height — 6 MillimeterAngle — 5 degree
Other devices from NuVasive, LLC
Properties
Other properties (12)
- 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
- Manufacturing Date: No