Leucadia Pedicle Screw System LG-CC1003
Listed
Valid until
Not applicable
FDA recalls
None ongoingDocuments
None
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00844856074279 | Date24 Sep 2014 | StatusListed |
Recalls
-
- Terminated Z-0155-2009
This action is being taken voluntarily as a result of a Warning Letter issued to AlIez Spine LLC by the Food & Drug Administration. The Company decided it could better address the FDA's concerns regarding Current Good Manufacturing Practice requirements of the Quality System without any product in the market so it could focus all of its efforts on responding to the FDA.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade Name
- Leucadia Pedicle Screw System
- Generic Name
- Bone-screw internal spinal fixation system connector
- Model / Reference
- LG-CC1003
- Primary DI / UDI-DI
- 00844856074279
- 510(k) Number
- FDA Product Code
- NKB, MNH, KWP, MNI, KWQ
- GMDN Term
- Bone-screw internal spinal fixation system connector
- Device Class
- Class II
- Regulation Number
- 888.3070, 888.3050, 888.3060
- GUDID distribution status
- Not in Commercial Distribution
- Sterilization Method
- Moist Heat or Steam Sterilization
- Size
- Width — 80 Millimeter
Other devices from Alphatec Spine, Inc.
Properties
Other properties (10)
- Sterile: 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