# K122156: Orthocon Absorbable Hemostatic Bone Putty

- Pathway: 510(k) (Traditional)
- Applicant: Orthocon, Inc.
- Decided: Jan 28, 2013 after 192 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). 14 ancestors in all.
3 later devices descend from it; 1 cites it directly.
1 of 18 devices in its family (counting itself) has a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K041363: Aoc Bone Wax, Ceremed, Inc. (2004) Summary page 1.
- K113079: Synthes Hemostatic Bone Putty, Synthes (Usa) Products, LLC/Norian Corporation (2011) Summary page 1.
- (no number) Ethicon Bone Wax: named in the summary without a submission number

## Most influential descendants
- K140117: Ahbppress Absorbable Hemostatic Bone Putty (2014), 2 descendants of its own
- K143069: HEMASORBPLUS press Resorable Hemostatic Bone Putty (2014), 0 descendants of its own
- K142339: HEMASORB Resorbable Hemostatic Bone Putty (2014), 0 descendants of its own

## Indications for use
Orthocon Absorbable Hemostatic Bone Putty is indicated for use as an absorbable implant material in the control of bleeding from bone surfaces.

Source page: https://510kreport.com/device/K122156
Methodology: https://510kreport.com/methodology