# K982420: Mitek Micro Anchor

- Pathway: 510(k) (Traditional)
- Applicant: Mitek Products
- Decided: Aug 24, 1998 after 70 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.
17 later devices descend from it; 6 cite it directly.
0 of 18 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) Suture: named in the summary without a submission number

## Most influential descendants
- K071520: Renovo Suture Anchors, Models 100-2001 Thru 100-5502X (2007), 7 descendants of its own
- K032078: Mitek Micro Quickanchor (2003), 5 descendants of its own
- K080352: Micro QA+ Anchor Witht #3-0 Orthocord Suture, Model 212843, Microfix AQ+ Anchor with #3-0 Orthocord Suture (2008), 4 descendants of its own
- K101126: Pontis Sutures and Suture Anchors with Optional Crimps (2010), 3 descendants of its own
- K110879: Biomet Sports Medicine Juggerknot (TM) Mini Soft Anchor (2011), 2 descendants of its own

## Indications for use
REPAIR/RECONSTRUCTION OF COLLATERAL LIGAMENTS, FLEXOR AND EXTENSION TENDONS AT THE PIP (PROXIMAL INTERPHALANGEAL), DIP (DISTAL INTERPHALANGEAL), AND MCP (METACARPAL INTERPHALANGEAL) JOINTS FOR ALL DIGITS

Source page: https://510kreport.com/device/K982420
Methodology: https://510kreport.com/methodology