FDA Product Code
FDA Product Code KTT — Clearance Directory
- Device Class
- Class II
- Assigned Panel
- Orthopedic
- 21 CFR Citation
- 888.3030
510(k) Clearances — 405 records · page 5 of 5
| K-Number | Device Name | Applicant | Decision Date | Clearance Type | Summary |
|---|---|---|---|---|---|
| K823548 | COMPRESSION HIP SCREW SIDE-PLATE | Howmedica Corp. | 1982-12-28 | Traditional | PDF ↗ |
| K813554 | ACE/KYLE CAPTURED HIP SCREW | Ace Orthopedic Manufacturing Co. | 1982-01-12 | Traditional | PDF ↗ |
| K811017 | HUCKSTEP INTRAMEDULLARY NAIL | Downs Surgical , Ltd. | 1981-05-27 | Traditional | PDF ↗ |
| K791619 | DYNAMIC HIP SCREW | Synthes (Usa) | 1979-08-28 | Traditional | PDF ↗ |
| K790501 | PEDIATRIC OSTEOTOMY SYSTEM | Howmedica Corp. | 1979-04-10 | Traditional | PDF ↗ |
Product code KTT · Class II · Orthopedic. Data: openFDA.