# K133770: A.I.M. Knotless Meniscal Repair Device

- Pathway: 510(k) (Traditional)
- Applicant: Anchor Innovation Medical (A.I.M.)
- Decided: Jun 10, 2014 after 181 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: 4 generations back to K925573 (1993). 5 ancestors in all.
No later device cites it as a predicate yet.
0 of 6 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K072322: Ultra Fast-Fix and Ultra Fast-Fix AB Meniscal Repair Systems, Smith & Nephew, Inc. (2007) Summary page 1.

## Indications for use
The A.I.M. Knotless Meniscal Repair Device is an implantable suture retention device which facilitates percutaneous or endoscopic soft tissue repair, including the repair of meniscal tears.

Source page: https://510kreport.com/device/K133770
Methodology: https://510kreport.com/methodology