# Vertebral Technologies, Inc.

- Location (FDA's records): Minneapolis, MN
- FDA decisions: 7 (2008–2013): 7 510(k) clearances
- Product codes: MAX (7)
- Predicates its devices cite: 10 (7 its own); citations of its devices by later devices: 11 (7 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
- Osteomed LP: 1 (https://510kreport.com/company/osteomed)
- Synthes Spine: 1 (https://510kreport.com/company/synthes-spine)
- Rsb Spine, LLC: 1 (https://510kreport.com/company/rsb-spine)

## Firms that cite its devices most
- Spineology, Inc.: 1 (https://510kreport.com/company/spineology)
- Zavation, LLC: 1 (https://510kreport.com/company/zavation)
- Globus Medical, Inc.: 1 (https://510kreport.com/company/globus-medical)
- Next Orthosurgical: 1 (https://510kreport.com/company/next-orthosurgical)

## Its most-cited devices
- K091988: Modification to: Interfuse Intervertebral Body Fusion Device , Model 9076 (2009), cited by 4
- K080673: Interfuse Intervertebral Body Fusion Device (2008), cited by 2
- K110226: Interfuse T Invertebral Body Fusion Device (2011), cited by 2
- K102277: Interfuse T Invertebral Body Fusion Device (2010), cited by 2
- K131540: Interfuse L Intervertebral Body Fusion Device (2013), cited by 1

## Recent decisions
- K131540: Interfuse L Intervertebral Body Fusion Device (Sep 3, 2013)
- K110226: Interfuse T Invertebral Body Fusion Device (May 27, 2011)
- K110045: Interfuse DA Invertebral Body Fusion Device (Feb 3, 2011)
- K102277: Interfuse T Invertebral Body Fusion Device (Oct 6, 2010)
- K093675: Interfuse Invertebral Body Fusion Device Model 9076 (Dec 23, 2009)
- K091988: Modification to: Interfuse Intervertebral Body Fusion Device , Model 9076 (Jul 30, 2009)
- K080673: Interfuse Intervertebral Body Fusion Device (Jun 10, 2008)

Source page: https://510kreport.com/company/vertebral-technologies