Depuy Motech Moss-Miami Spinal System
by Depuy, Inc. 510(k)
Active
510(k) K974573
Overview
The Depuy Motech Moss-Miami Spinal System is a spinal implant system intended for use in spinal fusion procedures. It is designed to provide stabilization and support for the spine during the healing process following surgical intervention.
The system is supplied as a non-sterile, reusable implant system composed of titanium components. It is indicated for use in orthopedic spinal surgery and has received FDA 510(k) clearance under product code KWP, with clearance granted on February 18, 1998.
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SN | NumberK974573 | Date18 Feb 1998 | StatusActive |
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not known
- Not covered
United States — FDA 510(k) Active
Recalls
No FDA recalls on record, checked 22 Oct 2026.
Specification
- 510(k) Number
- FDA Product Code
- KWP
- Device Class
- Class II
- Regulation
- 21 CFR Part 888.3050
- Advisory Committee
- Orthopedic
- FDA Decision
- SN
Other devices from Depuy, Inc.
Questions
What is the Depuy Motech Moss-Miami Spinal System used for?
The Depuy Motech Moss-Miami Spinal System is intended for use in spinal fusion procedures to provide stabilization and support for the spine during the healing process following surgical intervention in orthopedic spinal surgery.
How is the Depuy Motech Moss-Miami Spinal System supplied and is it sterile or reusable?
The system is supplied as a non-sterile, reusable implant system composed of titanium components, meaning it is not provided sterile and is designed for multiple uses after appropriate reprocessing.
What regulatory pathway was used for the Depuy Motech Moss-Miami Spinal System and when was it cleared?
The device received FDA 510(k) clearance under product code KWP, with a traditional clearance type, and the decision date was February 18, 1998, following receipt of the application on December 8, 1997.