# K001219: Memograph; Osstaple - Oral and Maxilliofacial Procedures for the Memograph Staple  System

- Pathway: 510(k) (Traditional)
- Applicant: Biomedical Ent., Inc.
- Decided: Jun 21, 2000 after 65 days
- Product code: JEY (Plate, Bone)
- Device class: 2
- Regulation: 21 CFR 872.4760
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
3 later devices descend from it; 3 cite it directly.
0 of 4 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
- K023488: Osstaple, Craniofacial (2002), 0 descendants of its own
- K023486: Osstaple, Maxillofacial (2002), 0 descendants of its own
- K023203: Osstaple (2002), 0 descendants of its own

Source page: https://510kreport.com/device/K001219
Methodology: https://510kreport.com/methodology