# K111524: MP 719

- Pathway: 510(k) (Traditional)
- Applicant: Marine Polymer Technologies, Inc.
- Decided: Jul 22, 2011 after 50 days
- Product code: MTJ (Wax, Bone)
- Device class: U
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 9 generations back to K791495 (1979). 34 ancestors in all.
No later device cites it as a predicate yet.
0 of 35 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K070557: MP 719, Marine Polymer Technologies, Inc. (2007) Summary page 1.
- K091636: Ostene CT, Aoc CT, Osteotene, Ceretene, Ceremed, Inc. (2009) Summary page 1.
- K063330: Orthocon Hemasorb Resorbable Hemostatic Bone Putty, Orthocon, Inc. (2006) Summary page 1.
- K971680: Auto Suture Bone Wax, United States Surgical, A Division of Tyco Healthc (1997) Summary page 1.

## Indications for use
MP719 is indicated for use as an implant material and for use in the control of bleeding from bone surfaces. The material may be used during surgical procedures and in treating traumatic injuries. MP719 is intended for use under the direction of a healthcare professional.

Source page: https://510kreport.com/device/K111524
Methodology: https://510kreport.com/methodology