Product code JDZ— Orthopedic
CEMENTRIFUGE
- Classification name
- Mixer, Cement, For Clinical Use
- Device class
- Class 1
- Regulation
- 21 CFR 888.4210
- Advisory panel
- Orthopedic
- Total cleared
- 13
- First cleared
- Most recent
Market context for product code JDZ
FDA has cleared devices under product code JDZ between 1976 and 1994, filed by 8 applicant companies. No FDA device recalls reference this product code. Class I devices are low-risk and subject to FDA general controls; many Class I device types are exempt from 510(k) premarket notification.
Clearances per year
- 1994
- 1991
- 1989
- 1986
- 1985
- 1984
- 1979
- 1978
- 1976
Top applicants under product code JDZ
Adverse events under product code JDZ
product code JDZ- Malfunction
- 461
- Total
- 461
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Recent clearances under product code JDZ
- K934253 — EXACTECH ALL POLY ACETABULAR CUP
- K925025 — PRISM BONE CEMENT MIXING SYSTEM
- K912190 — STRYKER HIGH VACUUM BONE CEMENT MIXER/INJECT SYST
- K892937 — REUSABLE BOWL AND SPATULA FOR MIXING BONE CEMENTS
- K861086 — ZIMMER VACUUM MIXING SYSTEM
- K854077 — MIX EVAC II
- K853310 — SIMPLEX ENHANCEMENT MIXER
- K851205 — CEMENTRIFUGE
- K843219 — ZIMMER BONE CEMENT CENTRIFUGATION SYS
- K792186 — HOWMEDICA MIX-KIT II
- K780857 — MIXING BOWL & SPATULA, DISPOSABLE
- K760617 — MIX EVAC BONE CEMENT
- K760636 — ORTHOMIX
Data sourced from openFDA. This site is unofficial and independent of the FDA.