# Apollo Spine, Inc.

- Location (FDA's records): Stoughton, MA
- FDA decisions: 7 (2009–2012): 7 510(k) clearances
- Names in FDA's records: Apollo Spine, Inc. (6); Apollo Spine (1)
- Product codes: KWQ (2), MNH (1), OVD (1), OVE (1), ODP (1), MRW (1)
- Predicates its devices cite: 9 (2 its own); citations of its devices by later devices: 6 (2 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
- Synthes (Usa): 2 (https://510kreport.com/company/synthes-usa)
- Howmedica Osteonics Corp.: 1 (https://510kreport.com/company/howmedica-osteonics)
- Sulzer Spine-Tech: 1 (https://510kreport.com/company/sulzer-spine-tech)
- Triage Medical, Inc.: 1 (https://510kreport.com/company/triage-medical)
- Amendia, Inc.: 1 (https://510kreport.com/company/amendia)
- X-Spine Systems, Inc.: 1 (https://510kreport.com/company/x-spine-systems)

## Firms that cite its devices most
- Providence Medical Technology, Inc.: 2 (https://510kreport.com/company/providence-medical-technology)
- Ldr Spine USA: 1 (https://510kreport.com/company/ldr-spine-usa)
- Spine Wave, Inc.: 1 (https://510kreport.com/company/spine-wave)

## Its most-cited devices
- K120340: Venus Facet Screw System (2012), cited by 4
- K101588: Eclipse Vertebral Spacer System-Cervical (2011), cited by 1
- K082504: Apollo Anterior Cervical Plate System (2009), cited by 1

## Recent decisions
- K120340: Venus Facet Screw System (Oct 19, 2012)
- K120143: Eclipse Vertebral Spacer System-Cervical (Feb 16, 2012)
- K102636: Zenith Pedicle System (Mar 3, 2011)
- K102121: Eclipse Vertebral Spacer System-Lumbar (Jan 12, 2011)
- K101588: Eclipse Vertebral Spacer System-Cervical (Jan 7, 2011)
- K090751: Comet Anterior Cervical Plate System (Oct 23, 2009)
- K082504: Apollo Anterior Cervical Plate System (Jan 27, 2009)

Source page: https://510kreport.com/company/apollo-spine