# K052799: Multitak 6.0 MM Absorbable Anchor System

- Pathway: 510(k) (Traditional)
- Applicant: Bonutti Research, Inc.
- Decided: Dec 16, 2005 after 74 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
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) Stryker BioZip Suture Anchor: named in the summary without a submission number
- (no number) Multitak suture anchors: named in the summary without a submission number

## Indications for use
The Multitak 6.0 mm Absorbable Anchor System consists of a single use absorbable anchor implant and is intended for use as a load bearing or non-load bearing suture anchor in the attachment of soft tissue to bone in various arthroscopic and open surgical procedures. The Multitak 6.0 mm Absorbable Anchor System is indicated for use in securing soft tissue to bone in such applications as the following: Shoulder: Bankart lesion repairs Acromio-clavicular repairs Deltoid repairs Rotator cuff tear repairs Biceps tenodesis SLAP lesion repairs Elbow, Wrist, & Hand: Scapholunate ligament reconstruction Ulnar collateral ligament reconstruction Radial collateral ligament reconstruction Biceps tendon reattachment Knee: Extra-capsular repairs Medial collateral ligament repair Lateral collateral ligament repair Posterior oblique ligament repair Illiotibial band tenodesis Patellar tendon repair VMO advancement Joint capsule closure Foot & Ankle: Medial instability repair/reconstruction Lateral instability repair/reconstruction Achilles instability repair/reconstruction Midfoot reconstruction Hallux valgus reconstruction Pelvis Bladder neck suspension procedures

Source page: https://510kreport.com/device/K052799
Methodology: https://510kreport.com/methodology