# K070033: Memometal Varisation, Models AV26-08, AV26-10, AV90-08 and AV90-10

- Pathway: 510(k) (Traditional)
- Applicant: Memometal Technologies
- Decided: Mar 19, 2007 after 75 days
- Product code: JDR (Staple, Fixation, Bone)
- 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.
16 later devices descend from it; 3 cite it directly.
0 of 17 devices 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) (DEPUY Inc) varisation staple: named in the summary without a submission number

## Most influential descendants
- K112794: Eos Small Bone Fixation System (2012), 9 descendants of its own
- K153395: OS2-C Compression Staple (2016), 7 descendants of its own
- K143323: OS2-V Varisation Staple (2015), 5 descendants of its own
- K153770: OS2(R)-VP Varisation Staple (2016), 4 descendants of its own
- K163440: Stealth Staple System (2017), 3 descendants of its own

## Indications for use
The MEMOMETAL varisation staples (AV XX-YY) are indicated for Akin type osteotomies

Source page: https://510kreport.com/device/K070033
Methodology: https://510kreport.com/methodology