Restore Tunnel Plug
by Depuy, Inc. 510(k)
Active
510(k) K923069
Overview
The Restore Tunnel Plug is an orthopedic device designed for use in surgical procedures. It functions as a tunnel plug to assist in orthopedic applications.
This device is identified by K-number K923069 and has received FDA 510(k) clearance. It is manufactured by Depuy, Inc. and is categorized under the orthopedic advisory committee.
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SESE | NumberK923069 | Date8 Jun 1993 | 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- Withdrawn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
- HRX
- Device Class
- Class II
- Regulation
- 21 CFR Part 888.1100
- Advisory Committee
- Orthopedic
- FDA Decision
- SESE Substantially Equivalent
Other devices from Depuy, Inc.
Questions
What is the primary function of the Restore Tunnel Plug?
The Restore Tunnel Plug is an orthopedic device specifically engineered to function as a tunnel plug, providing support and assistance during various orthopedic surgical procedures.
What is the regulatory status of this device?
The Restore Tunnel Plug has received FDA 510(k) clearance under the K-number K923069. This indicates that the device has been determined to be substantially equivalent to legally marketed predicate devices.
Who is the manufacturer of the Restore Tunnel Plug?
The device is manufactured by Depuy, Inc., which is based in Warsaw, Indiana. The company submitted the device for review under the orthopedic advisory committee.