# K993373: Rotorblade Suture Anchor

- Pathway: 510(k) (Special)
- Applicant: Li Medical Technologies, Inc.
- Decided: Oct 27, 1999 after 20 days
- Product code: MAI (Fastener, Fixation, Biodegradable, Soft Tissue)
- Device class: 2
- Regulation: 21 CFR 888.3030
- 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 K950272 (1996). 3 ancestors in all.
No later device cites it as a predicate yet.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K983435: Rotorblade, Li Medical Technologies, Inc. (1999) Summary page 1.
- K992938: Rotorblade Suture Anchor, Li Medical Technologies, Inc. (1999) Summary page 1.

## Indications for use
Shoulder: rotator cuff repair

Source page: https://510kreport.com/device/K993373
Methodology: https://510kreport.com/methodology