# K920213: Mitek Anchor, Mitek Anchor II

- Pathway: 510(k) (Traditional)
- Applicant: Mitek Surgical Products, Inc.
- Decided: May 1, 1992 after 106 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.
109 later devices descend from it; 7 cite it directly.
0 of 110 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K960825: LM Anchor or Other Proprietary Name (1996), 61 descendants of its own
- K960439: LM Bone Anchor (1996), 60 descendants of its own
- K963812: LM Bone Anchor (Orthopedics) (1996), 58 descendants of its own
- K091549: Conmed Linvatec Soft Tissue to Bone System (2009), 56 descendants of its own
- K962372: Urotac Bone Anchor Inserter (1996), 44 descendants of its own

Source page: https://510kreport.com/device/K920213
Methodology: https://510kreport.com/methodology