Dtt System
by Depuy, Inc. 510(k)
Active
510(k) K790404
Overview
At Depuy, Inc., we have been dedicated to developing innovative medical devices for orthopedic care since the early 1970s. Our flagship product, the DTT System, is a revolutionary implantable joint replacement solution that has undergone rigorous clinical testing and regulatory approval. With its unique design and advanced materials, this device offers unparalleled performance and durability, making it an industry leader in its field.
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SESE | NumberK790404 | Date21 Mar 1979 | StatusActive |
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- 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
- KWQ
- Device Class
- Class II
- Regulation
- 21 CFR Part 888.3060
- Advisory Committee
- Orthopedic
- FDA Decision
- SESE Substantially Equivalent