# K153317: HEMASORBPLUS Resorbable Hemostatic Bone Putty

- Pathway: 510(k) (Traditional)
- Applicant: Orthocon, Inc.
- Decided: Nov 30, 2016 after 378 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: 8 generations back to K791495 (1979). 14 ancestors in all.
No later device cites it as a predicate yet.
0 of 15 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K123243: Hemasorb Bone Putty 3 Resorbable Hemostatic Bone Putty, Orthocon, Inc. (2013) Summary page 4.

## Indications for use
Orthocon HemasorbPlus Resorbable Hemostatic Bone Putty is indicated for the control of bleeding from cut or damaged bone by acting as a mechanical barrier or tamponade.

Source page: https://510kreport.com/device/K153317
Methodology: https://510kreport.com/methodology