# K132268: Quill Pdo Knotless Tissue-Closure Device, Variable Loop Design

- Pathway: 510(k) (Special)
- Applicant: Surgical Specialties Corporation Dba Angiotech
- Decided: Aug 23, 2013 after 32 days
- Product code: NEW (Suture, Surgical, Absorbable, Polydioxanone)
- Device class: 2
- Regulation: 21 CFR 878.4840
- 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 K014153 (2002). 19 ancestors in all.
No later device cites it as a predicate yet.
0 of 20 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K113744: Quill Pdo Knotless Tissue-Closure Device (Polydioxanone), Angiotech (2012) Summary page 1.
- K123877: Quill Pdo Knotless Tissue-Closure Device, Variable Loop Design, Surgical Specialties Corp. Dba Angiotech (2013) Summary page 1.

## Indications for use
QuilT M PDO Knotless Tissue-Closure Device comprised of Polydioxanone, is indicated for soft tissue approximation where use of an absorbable suture is appropriate.

Source page: https://510kreport.com/device/K132268
Methodology: https://510kreport.com/methodology