# K023963: Adhoc Claw

- Pathway: 510(k) (Traditional)
- Applicant: Future Medical Systems, Inc.
- Decided: May 5, 2003 after 157 days
- Product code: MBI (Fastener, Fixation, Nondegradable, Soft Tissue)
- 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: 1 generation back to K884565 (1989). 3 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 5 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K953877: Mitek Gii Anchor, Mitek Surgical Products, Inc. (1995) Summary page 1.
- K884565: Acufex Fixation Button, Acufex Microsurgical, Inc. (1989) Summary page 1.
- K896310: Acufex Fixation Button; Retention Bar, Wedge, Acufex Microsurgical, Inc. (1989) Summary page 1.

## Most influential descendants
- K024185: Biodhoc (2004), 0 descendants of its own

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

Source page: https://510kreport.com/device/K023963
Methodology: https://510kreport.com/methodology