# K223582: MectaLock TI Triple Loaded Suture Anchor

- Pathway: 510(k) (Traditional)
- Applicant: Medacta International S.A.
- Decided: Feb 24, 2023 after 85 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: 3 generations back to K003984 (2001). 9 ancestors in all.
2 later devices descend from it; 1 cites it directly.
0 of 12 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K191300: MectaLock Ti Suture Anchor, Medacta International S.A. (2019) Summary page 4.

## Most influential descendants
- K230544: SnugFit All-Suture Anchor extension (2023), 1 descendant of its own
- K251933: SnugFit ASA Extension (2025), 0 descendants of its own

## Indications for use
The MectaLock TI Triple Loaded Suture Anchors are intended for use in arthroscopic or open surgical approaches for fixation of suture (soft tissue) to bone in shoulder in the following procedure: - Shoulder: rotator cuff repair and biceps tenodesis.

Source page: https://510kreport.com/device/K223582
Methodology: https://510kreport.com/methodology