# K020221: Iql Basic Fragment Plate Set, Iql Basic Fragment Screw Set, Iql Small Fragment Set, Iql Mini Fragment Set

- Pathway: 510(k) (Traditional)
- Applicant: Biomet Orthopedics, Inc.
- Decided: Apr 2, 2002 after 70 days
- Product code: HRS (Plate, Fixation, Bone)
- Device class: 2
- Regulation: 21 CFR 888.3030
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
23 later devices descend from it; 5 cite it directly.
0 of 24 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) Various stainless steel bone plates and screws sold by Biomet Inc. (OEC) prior to May 28, 1976: named in the summary without a submission number

## Most influential descendants
- K090666: Pediplates (2009), 15 descendants of its own
- K100240: Orthopediatrics Pediloc Tibia Plate System (2010), 13 descendants of its own
- K111086: Orthopediatrics Fracture and Osteotomy Bone Plate System (2011), 7 descendants of its own
- K093761: Optilock VL (Variable Angle Locking) Distal Radius Plating System (2010), 3 descendants of its own
- K192181: PRECICE Plating System (2019), 2 descendants of its own

## Indications for use
IQL Bone Plates and Screws are used for adult or pediatric patients as indicated for pelvic, small and long bone fracture fixation and fixation of bones that have been surgically prepared (osteatomy) for correction of deformity or arthrodesis. Indications for use include internal fixation of the tibia, fibula, femur, metacarpals, metatarsals, humerus, ulna, radius, middle hand and middle foot bones.

Source page: https://510kreport.com/device/K020221
Methodology: https://510kreport.com/methodology