# K203186: DYNATAPE Suture

- Pathway: 510(k) (Traditional)
- Applicant: Medos International SARL
- Decided: Mar 18, 2021 after 142 days
- Product code: GAT (Suture, Nonabsorbable, Synthetic, Polyethylene)
- Device class: 2
- Regulation: 21 CFR 878.5000
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 6 generations back to K990088 (1999). 13 ancestors in all.
No later device cites it as a predicate yet.
0 of 14 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K181182: DYNACORD Suture, Medos International SARL (2018) Summary page 4.

## Indications for use
DYNATAPE suture is indicated for orthopedic procedural use in soft-tissue approximation, and/ or ligation, including use with allograft tissue.

Source page: https://510kreport.com/device/K203186
Methodology: https://510kreport.com/methodology