Product code MQP— Orthopedic

MODIFICATION TO VERTE-STACK SPINAL SYSTEM

Classification name
Spinal Vertebral Body Replacement Device
Device class
Class 2
Regulation
21 CFR 888.3060
Advisory panel
Orthopedic
Total cleared
279
First cleared
Most recent

Market context for product code MQP

FDA has cleared 279 devices under product code MQP between 1999 and 2026, filed by 108 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

last 15 years

Top applicants under product code MQP

Adverse events under product code MQP

product code MQP
Injury
372
Malfunction
519
Total
891

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 MQP

1–100 of 279

Data sourced from openFDA. This site is unofficial and independent of the FDA.