CoRoent 6090930
Active
Valid until
No expiry
FDA recalls
None foundDocuments
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SESE | NumberK231735 | Date11 Jul 2023 | StatusActive |
| United States | GUDID listing | Number00887517288578 | Date24 Oct 2015 | StatusListed |
Recalls
No FDA recalls found in the data synced 9 Nov 2026.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- CoRoent
- Generic name
- Metallic spinal interbody fusion cage
- Model / reference
- 6090930
- Primary DI / UDI-DI
- 00887517288578
- 510(k) Number
- FDA product code
- MQP, MAX, ODP, PHM, OVD
- GMDN term
- Metallic spinal interbody fusion cage
- Device class
- Class II
- Regulation number
- 888.3060, 888.3080
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
Overview
AI-generated summary, 9 Nov 2026
The CoRoent 6090930 is a Spinal Vertebral Body Replacement Device, specifically a metallic spinal interbody fusion cage. This device is identified as CoRoent LO Ti, measuring 9x10x30mm with a 10° angle. It must be sterilized prior to use, with moist heat or steam sterilization as the recommended methods.
This device received multiple 510(k) clearances, including K120918, K140319, K140659, K141665, K141896, K150994, K151472, K153419, K160916, K161230, K163707, K170962, and K231735. It is a Class II device with product codes MQP (regulation 888.3060), MAX (regulation 888.3080), ODP (regulation 888.3080), PHM (regulation 888.3080), and OVD (regulation 888.3080).
Other devices from NuVasive, LLC
Questions
AI-generated answers, 9 Nov 2026
What is the CoRoent 6090930?
It is recorded under the GMDN device type "Metallic spinal interbody fusion cage", which GMDN defines as "A device intended to be implanted into the space of an intervertebral disc that has been partially or totally removed during surgery in order to allow bone fusion between two contiguous vertebral bodies, typically in the treatment of degenerative disc disease (DDD)". FDA lists it under the product name "Spinal Vertebral Body Replacement Device". It is recorded as Class II.
What are the product code and regulation of the CoRoent 6090930?
FDA records the CoRoent 6090930 under product code MQP and regulation number 888.3060.
Who makes the CoRoent 6090930?
NuVasive, LLC is the manufacturer on record for the CoRoent 6090930.
Properties
Other properties (11)
- Supplied sterile: No
- Single use: 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