Product code JDP— Orthopedic
4.5MM VA-LCP CURVED CONDYLAR PLATE SYSTEM
- Classification name
- Condylar Plate Fixation Implant
- Device class
- Class 2
- Regulation
- 21 CFR 888.3030
- Advisory panel
- Orthopedic
- Total cleared
- 2
- First cleared
- Most recent
Market context for product code JDP
FDA has cleared devices under product code JDP between 2011 and 2017, filed by 2 applicant companies. No FDA device recalls reference this product code. Class II devices are moderate-risk and subject to general and special controls; most reach market through 510(k) clearance by demonstrating substantial equivalence to a predicate device.
Clearances per year
- 2017
- 2011
Top applicants under product code JDP
Adverse events under product code JDP
product code JDP- Injury
- 206
- Total
- 206
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 JDP
Data sourced from openFDA. This site is unofficial and independent of the FDA.