# K110800: Meta-Lock Suture Anchor System

- Pathway: 510(k) (Traditional)
- Applicant: Tarsus Medical, Inc.
- Decided: Sep 27, 2011 after 189 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: 3 generations back to K915889 (1992). 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)
- K051989: Gii Quickanchor Plus with Orthocord Suture, Depuy Mitek, A Johnson & Johnson Company (2005) Summary page 1.

## Indications for use
The Tarsus Medical Meta-Lock Suture Anchor System is intended for fixation of suture to bone for the indications listed below: SHOULDER: Bankart repair, SLAP lesion repair, acromio-clavicular separation, rotator cuff repair, capsule shift/capsulo-labral reconstruction, biceps tenodesis; deltoid repair ANKLE: Lateral instability, medial instability, achilles tendon repair/reconstruction, midfoot reconstructions FOOT: Hallux valgus reconstruction WRIST: Scapholunate ligament HAND: Ulnar or lateral collateral ligament reconstruction ELBOW: Biceps tendon reattachment KNEE: Extra capsular repairs; reattachment of: medial collateral ligament, lateral collateral ligament, posterior oblique ligament or joint capsule to tibia and joint capsule closure to anterior proximal tibia; extra capsular reconstruction, ITB tendonesis; patellar ligament and tendon avulsions.

Source page: https://510kreport.com/device/K110800
Methodology: https://510kreport.com/methodology