# Anatomica AB

- Location (FDA's records): Washington, DC
- FDA decisions: 1 (2007–2007): 1 510(k) clearance
- Product codes: KWP (1)
- Predicates its devices cite: 2 (0 its own); citations of its devices by later devices: 1 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Interpore Cross Intl.: 2 (https://510kreport.com/company/interpore-cross-intl)

## Firms that cite its devices most
- Omni Surgical, LLC Dba Spine360: 1 (https://510kreport.com/company/omni-surgical-dba-spine360)

## Its most-cited devices
- K061943: Anatomica Posterior Cervical Fixation System (2007), cited by 1

## Recent decisions
- K061943: Anatomica Posterior Cervical Fixation System (May 25, 2007)

Source page: https://510kreport.com/company/anatomica