# K102339: Conmed Linvatec Sequent Meniscal Repair Device

- Pathway: 510(k) (Traditional)
- Applicant: Conmed Linvatec
- Decided: Nov 23, 2010 after 97 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: 5 generations back to K925573 (1993). 6 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 8 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K073149: Meniscal Cinch, Arthrex, Inc. (2008) Summary page 1.
- K072322: Ultra Fast-Fix and Ultra Fast-Fix AB Meniscal Repair Systems, Smith & Nephew, Inc. (2007) Summary page 1.

## Most influential descendants
- K220186: Zone Specific AIM (2022), 0 descendants of its own

## Indications for use
The ConMed Linvatec SequentTM Meniscal Repair Device is an implantable suture retention device which facilitates percutaneous or endoscopic soft tissue repairs, including the repair of meniscal tears.

Source page: https://510kreport.com/device/K102339
Methodology: https://510kreport.com/methodology