# K963587: Wright Plaster of Paris Bone Void Filler Kit (Subject to Revision)

- Pathway: 510(k) (Traditional)
- Applicant: Wrightmedicaltechnologyinc
- Decided: Mar 24, 1997 after 196 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.
13 later devices descend from it; 4 cite it directly.
0 of 14 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) Wright Plaster of Paris Pellets: named in the summary without a submission number

## Most influential descendants
- K991854: Osteoplast, Model POP200 (1999), 9 descendants of its own
- K013790: Calcigen-S Bone Void Filer (2002), 6 descendants of its own
- K031319: Osteo-G Bone Void Filler System (2003), 4 descendants of its own
- K033258: Bonesave Bone Void Filler (2004), 3 descendants of its own
- K091688: A-Grix Resorbable Bone Void Filler (2010), 1 descendant of its own

## Indications for use
Wright Plaster of Paris Pellets are intended to be gently packed into non-loadbearing voids in long bone. These bone voids may be surgically created osseous defects or osseous defects created from traumatic, injury to the bone. The pellets provide a bone void filler that resorbs and is replaced with bone during the healing process.

Source page: https://510kreport.com/device/K963587
Methodology: https://510kreport.com/methodology