# K220186: Zone Specific AIM

- Pathway: 510(k) (Traditional)
- Applicant: Conmed Corporation
- Decided: May 13, 2022 after 109 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 K925573 (1993). 7 ancestors in all.
No later device cites it as a predicate yet.
0 of 8 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K102339: Conmed Linvatec Sequent Meniscal Repair Device, Conmed Linvatec (2010) Summary page 4.

## Indications for use
The Zone Specific AIM™ Device is an implantable suture retention device which facilitates percutaneous or endoscopic soft tissue repairs, including repair of meniscal tears.

Source page: https://510kreport.com/device/K220186
Methodology: https://510kreport.com/methodology