# Next Orthosurgical

- Location (FDA's records): Vista, CA
- FDA decisions: 6 (2013–2024): 6 510(k) clearances
- Product codes: NKB (3), MAX (2), ODP (1)
- 510(k) review time since 2016: median 85 days, against 88 for FDA's reviews in the same codes and years (2 of 4 faster)
- Predicates its devices cite: 27 (3 its own); citations of its devices by later devices: 6 (3 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
- Spinal Elements, Inc.: 3 (https://510kreport.com/company/spinal-elements)
- Synthes Spine: 3 (https://510kreport.com/company/synthes-spine)
- Depuyacromed: 2 (https://510kreport.com/company/depuyacromed)
- Medtronic Sofamor Danek: 2 (https://510kreport.com/company/medtronic-sofamor-danek)
- Nuvasive, Inc.: 2 (https://510kreport.com/company/nuvasive)
- Medos International SARL: 1 (https://510kreport.com/company/medos-international)
- Ebi, L.P.: 1 (https://510kreport.com/company/ebi)
- Vertebral Technologies, Inc.: 1 (https://510kreport.com/company/vertebral-technologies)

## Firms that cite its devices most
- Astura Medical: 1 (https://510kreport.com/company/astura-medical)
- Nuvasive, Inc.: 1 (https://510kreport.com/company/nuvasive)
- Pinnacle Spine Group, LLC: 1 (https://510kreport.com/company/pinnacle-spine-group)

## Its most-cited devices
- K131082: Interform Interbody Cage System (2013), cited by 3
- K141291: Vertiform Posterior Fixation System (2014), cited by 2
- K161499: VertiForm Posterior Fixation System (2016), cited by 1

## Recent decisions
- K242509: HAnano InterFuse (R) Modular Interbody (Sep 19, 2024)
- K190981: NEX-D2 Posterior Fixation System (Jan 15, 2020)
- K161608: InterForm Cervical Interbody Cage System (Sep 30, 2016)
- K161499: VertiForm Posterior Fixation System (Jul 29, 2016)
- K141291: Vertiform Posterior Fixation System (Aug 26, 2014)
- K131082: Interform Interbody Cage System (Aug 26, 2013)

Source page: https://510kreport.com/company/next-orthosurgical