# Creaspine

- Location (FDA's records): North Attleboro, MA
- FDA decisions: 3 (2007–2008): 3 510(k) clearances
- Names in FDA's records: Creaspine (2); Creaspine Sas (1)
- Product codes: MQP (3)
- Predicates its devices cite: 9 (1 its own); citations of its devices by later devices: 1 (1 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
- Depuyacromed: 3 (https://510kreport.com/company/depuyacromed)
- United States Surgical, A Division of Tyco Healthc: 3 (https://510kreport.com/company/united-states-surgical-a-division-of-tyco-healthc)
- Spine Wave, Inc.: 1 (https://510kreport.com/company/spine-wave)
- Theken Spine, LLC: 1 (https://510kreport.com/company/theken-spine)

## Its most-cited devices
- K072537: Creaspine Supstance Vertebral Body Replacement System (2007), cited by 1

## Recent decisions
- K081564: Creaspine Supstance Vertebral Body Replacement System Line Extension (Jun 30, 2008)
- K080860: Creaspine Supstance Small Vertebral Body Replacement System (May 29, 2008)
- K072537: Creaspine Supstance Vertebral Body Replacement System (Dec 18, 2007)

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