# K071941: Memometal Bone Anchors

- Pathway: 510(k) (Traditional)
- Applicant: Memometal Technologies
- Decided: Dec 4, 2007 after 144 days
- Product code: HWC (Screw, Fixation, Bone)
- 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: 2 generations back to K921873 (1992). 4 ancestors in all.
No later device cites it as a predicate yet.
0 of 5 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K992487: Mitek Mini Quickanchor Plus, Mitek Products (1999) Summary page 1.

## Indications for use
The MEMOMETAL Micro ARIM® is indicated for - Hand: ligament reconstruction - Ankle: Midfoot reconstruction - Foot: Hallux Valgus reconstruction - Wrist: Scapholunate Ligament reconstruction - Pubis: Fixation in the pubis for bladder neck suspension to resolve stress urinary incontinence

Source page: https://510kreport.com/device/K071941
Methodology: https://510kreport.com/methodology