JDQ
- Product code
- JDQ
- Device name
- Cerclage, Fixation
- Device class
- Class 2
- 21 CFR
- 21 CFR 888.3010
- Medical specialty
- Orthopedic
- Marketing pathway
- 510(K)
- Flag
- Implant
- 510(k) clearances (last 3 years)
- 6
- Summaries archived here
- 5 (direct download)
- 510(k) clearances (all years, FDA)
- 130 (all years; only the last 3 years are listed here)
510(k) clearances, last 3 years (6)
| Number | Decision date | Applicant | Device name | Summary |
|---|---|---|---|---|
| K261271 | 2026-07-16 | Pioneer Surgical Technology, Inc. | Cable-Ready® Cable Grip System | |
| K243905 | 2025-08-14 | GM Dos Reis Industria e Comercio Ltda. | Stitch Cerclage Suture Tapes | |
| K243344 | 2025-02-20 | Arthrex, Inc. | Arthrex FiberTape and TigerTape Cerclage Sutures; Ar… | |
| K232733 | 2024-05-03 | Medacta International S.A. | Mbrace Cable | FDA |
| K233949 | 2024-03-13 | Smith & Nephew, Inc. | ACCORD Cable System | |
| K232986 | 2024-01-30 | Circumfix Solutions, Inc. | VariTrax Sternal CircumFixation System |
Official FDA classification page: JDQ
Classification and pathway per current FDA publications. Data from openFDA (CC0).