# K203485: SnugFit All-Suture Anchor

- Pathway: 510(k) (Traditional)
- Applicant: Medacta International S.A.
- Decided: Jan 19, 2021 after 53 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: 10 generations back to K792022 (1979). 61 ancestors in all.
2 later devices descend from it; 2 cite it directly.
0 of 64 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K150768: JuggerKnot Soft Anchors, Biomet Manufacturing Corp (2015) Summary page 4.
- K193461: MectaLock All-Suture Anchors, Medacta International S.A. (2020) 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 SnugFit All-Suture Anchor is intended for use in arthroscopic or open surgical approaches for fixation of soft tissue to bone in the hip and shoulder in the following procedures: - Hip: acetabular labral repair - Shoulder: glenoid labrum repair; rotator cuff repair, biceps tendon repair

Source page: https://510kreport.com/device/K203485
Methodology: https://510kreport.com/methodology