# Altus Partners, LLC

- Location (FDA's records): West Chester, PA
- FDA decisions: 18 (2013–2025): 18 510(k) clearances
- Names in FDA's records: Altus Partners, LLC (17); Altus Partners (1)
- Product codes: NKB (6), MAX (5), KWQ (2), MNI (1), NKG (1), OLO (1), ODP (1), OVD (1)
- 510(k) review time since 2016: median 160 days, against 96 for FDA's reviews in the same codes and years (2 of 16 faster)
- Predicates its devices cite: 53 (17 its own); citations of its devices by later devices: 24 (17 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
- Vertebron, Inc.: 15 (https://510kreport.com/company/vertebron)
- Corelink, LLC: 2 (https://510kreport.com/company/corelink)
- Zimmer Spine, Inc.: 1 (https://510kreport.com/company/zimmer-spine)
- Synthes (Usa): 1 (https://510kreport.com/company/synthes-usa)
- Theken Spine, LLC: 1 (https://510kreport.com/company/theken-spine)
- Medtronic Sofamor Danek: 1 (https://510kreport.com/company/medtronic-sofamor-danek)
- Altus Spine: 1 (https://510kreport.com/company/altus-spine)
- U&I Corp., America: 1 (https://510kreport.com/company/u-i-america)

## Firms that cite its devices most
- OsteoCentric Technologies: 2 (https://510kreport.com/company/osteocentric-technologies)
- Altus Spine: 2 (https://510kreport.com/company/altus-spine)
- Nanovis, LLC: 1 (https://510kreport.com/company/nanovis)
- U&I Corporation: 1 (https://510kreport.com/company/u-i)
- Bk Meditech, Co., Ltd.: 1 (https://510kreport.com/company/bk-meditech)

## Its most-cited devices
- K181339: Altus Spine Pedicle Screw System (2018), cited by 4
- K160976: Altus Spine Interbody Fusion System (2017), cited by 4
- K151648: Altus Spine Pedicle Screw System, Altus Spine MIS Pedicle Screw System, Valencia Pedicle Screw System, Valencia MIS Pedicle Screw System (2015), cited by 3
- K170512: Altus Spine Titanium Interbody Fusion System (2017), cited by 3
- K132280: Altus Spine Pedicle Screw System (2013), cited by 2
- K200322: Altus Spine Pedicle Screw System (2020), cited by 2

## Recent decisions
- K243419: Altus Spine Navigation System (May 8, 2025)
- K211027: Altus Spine Pedicle Screw System (Sep 16, 2022)
- K211837: Altus Spine Interbody Standalone Fusion System (Apr 19, 2022)
- K210887: Altus Spine Sochi OCT Spinal System (Aug 20, 2021)
- K200922: Altus Spine HA Pedicle Screw System (Jan 26, 2021)
- K200322: Altus Spine Pedicle Screw System (Jun 2, 2020)
- K183084: Fuji Cervical Plate System (May 29, 2019)
- K182406: Altus Spine Interbody Fusion System (Feb 22, 2019)

Source page: https://510kreport.com/company/altus-partners