QBO

Instruments Designed For Press-Fit Osteochondral Implants

Product code: QBO
Device name: Instruments Designed For Press-Fit Osteochondral Implants
Device class: Class 2
21 CFR: 21 CFR 888.4505
Medical specialty: Orthopedic
Marketing pathway: 510(K) Exempt
510(k) clearances (last 3 years): 2

FDA classification definition

The device is intended to manipulate bone and cartilage tissue or implant materials for the positioning, alignment, defect creation, or placement of press-fit osteochondral implants.

Definition text from the FDA device classification database (U.S. federal government work, public domain).

Official FDA classification page: QBO

Classification and pathway per current FDA publications. Data from openFDA (CC0).