# K024185: Biodhoc

- Pathway: 510(k) (Traditional)
- Applicant: Future Medical Systems, SA
- Decided: Jan 15, 2004 after 392 days
- Product code: HTY (Pin, Fixation, Smooth)
- Device class: 2
- Regulation: 21 CFR 888.3040
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 2 generations back to K884565 (1989). 5 ancestors in all.
No later device cites it as a predicate yet.
0 of 6 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K991009: RC Buttress, Biomet, Inc. (1999) Summary page 1.
- K023963: Adhoc Claw, Future Medical Systems, Inc. (2003). Cleared while this submission was under review Summary page 1.

## Indications for use
The BIODHOC is an implant used for rotator cuff repair in shoulder surgery.

Source page: https://510kreport.com/device/K024185
Methodology: https://510kreport.com/methodology