# Interventional Spine, Inc.

- Location (FDA's records): Irvine, CA
- FDA decisions: 8 (2008–2016): 8 510(k) clearances
- Product codes: MAX (6), MRW (2)
- Predicates its devices cite: 12 (4 its own); citations of its devices by later devices: 16 (4 its own)
- Recalls linked to its devices: 2 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Globus Medical, Inc.: 3 (https://510kreport.com/company/globus-medical)
- Triage Medical, Inc.: 2 (https://510kreport.com/company/triage-medical)
- Kiscomedica S.A.: 2 (https://510kreport.com/company/kiscomedica)
- Trans1 Incorporated: 1 (https://510kreport.com/company/trans1)

## Firms that cite its devices most
- Medos International SARL: 3 (https://510kreport.com/company/medos-international)
- Spinal Elements, Inc.: 2 (https://510kreport.com/company/spinal-elements)
- Life Spine, Inc.: 1 (https://510kreport.com/company/life-spine)
- Spine Wave, Inc.: 1 (https://510kreport.com/company/spine-wave)
- Osteomed LP: 1 (https://510kreport.com/company/osteomed)
- Alphatec Spine, Inc.: 1 (https://510kreport.com/company/alphatec-spine)
- X-Spine Systems, Inc.: 1 (https://510kreport.com/company/x-spine-systems)
- Depuy Spine, Inc.: 1 (https://510kreport.com/company/depuy-spine)

## Its most-cited devices
- K113527: Opticage Interbody Fusion Device (2012), cited by 8
- K090767: Perpos FCD-2 System (Single Patient Use), Anchor, Stabilizer (2009), cited by 2
- K082795: Single Use Perpos PLS System, 4.5 Bone-Lok PLS Implant (2008), cited by 2
- K152156: Opticage Expandable Interbody Fusion Device (2015), cited by 2
- K160464: Opticage (R) Expandable Interbody Fusion Device (2016), cited by 1
- K132479: Opticage Interbody Fusion Device, Model 9080-00 (2013), cited by 1

## Recent decisions
- K160464: Opticage (R) Expandable Interbody Fusion Device (Apr 4, 2016)
- K152156: Opticage Expandable Interbody Fusion Device (Oct 19, 2015)
- K140716: Opticage Expandable Interbody Fusion Device (Nov 24, 2014)
- K133583: Opticage Interbody Fusion Device, Model Series 9070 (Feb 10, 2014)
- K132479: Opticage Interbody Fusion Device, Model 9080-00 (Sep 19, 2013)
- K113527: Opticage Interbody Fusion Device (Jan 20, 2012)
- K090767: Perpos FCD-2 System (Single Patient Use), Anchor, Stabilizer (Jun 11, 2009)
- K082795: Single Use Perpos PLS System, 4.5 Bone-Lok PLS Implant (Dec 12, 2008)

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