# K023922: Coapt Systems Endotine Device, Model CFD-101-00197

- Pathway: 510(k) (Special)
- Applicant: Coapt Systems, Inc.
- Decided: Dec 20, 2002 after 25 days
- Product code: HWC (Screw, Fixation, Bone)
- 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 K014153 (2002). 1 ancestor in all.
81 later devices descend from it; 6 cite it directly.
0 of 83 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K014153: Coapt Systmes Endotine Device, Coapt Systems, Inc. (2002)

## Most influential descendants
- K032698: Coapt Endotine Midface-ST 4.5 Device (2003), 74 descendants of its own
- K041593: Featherlift Extended Length Aptos Thread (2004), 72 descendants of its own
- K050548: Contour Midface Opposing Uni-Directional Threads (2005), 65 descendants of its own
- K051609: Quill Synthetic Absorbable Barbed Suture (2005), 64 descendants of its own
- K071989: Quill Self-Retaining System (SRS) Synthetic Absorbable Surgical Suture Material (2007), 31 descendants of its own

## Indications for use
The ENDOTINE Device is intended for use in browplasty surgery. The ENDOTINE device is specifically intended for use to fixate the subdermis to the cranial bone in browplasty procedures.

Source page: https://510kreport.com/device/K023922
Methodology: https://510kreport.com/methodology