DeviceClearance

Product code MQV— Orthopedic

MagnetOs Putty

Classification name
Filler, Bone Void, Calcium Compound
Device class
Class 2
Regulation
21 CFR 888.3045
Advisory panel
Orthopedic
Total cleared
492
First cleared
Most recent

Market context for product code MQV

FDA has cleared 492 devices under product code MQV between 1996 and 2026, filed by 183 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 MQV

Adverse events under product code MQV

product code MQV
Death
6
Injury
435
Total
441

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 MQV

1–100 of 492

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