# K011531: Calcium Phosphate Granular Bone Void Filler

- Pathway: 510(k) (Traditional)
- Applicant: Biomet, Inc.
- Decided: Sep 6, 2002 after 477 days
- Product code: MQV (Filler, Bone Void, Calcium Compound)
- Device class: 2
- Regulation: 21 CFR 888.3045
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
16 later devices descend from it; 2 cite it directly.
0 of 17 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K050025: Nanoss Bone Void Filler (2005), 11 descendants of its own
- K081558: Pioneer Surgical Technology Nanoss BVF-E, Models 5, 10, 20CC (2008), 10 descendants of its own
- K091031: Pioneer Surgical Nanoss BVF-E (2009), 7 descendants of its own
- K110561: Fortross Bone Void Filler (2011), 4 descendants of its own
- K141600: Nanoss Bioactive, Nanoss Bioactive Loaded, and Nanoss Bioactive Loaded Kit (2014), 3 descendants of its own

Source page: https://510kreport.com/device/K011531
Methodology: https://510kreport.com/methodology