# New Business Development, LLC

- Location (FDA's records): Woodstock, GA
- FDA decisions: 4 (2002–2007): 4 510(k) clearances
- Product codes: MQP (1), HAW (1), GXI (1), JDK (1)
- Predicates its devices cite: 2 (0 its own); citations of its devices by later devices: 1 (0 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
- Elekta Instrument AB: 1 (https://510kreport.com/company/elekta-instrument)
- Signus Medizintechnik GmbH: 1 (https://510kreport.com/company/signus-medizintechnik)

## Firms that cite its devices most
- Amendia, Inc.: 1 (https://510kreport.com/company/amendia)

## Its most-cited devices
- K072029: Phenix Vertebral Body Replacement (2007), cited by 1

## Recent decisions
- K072029: Phenix Vertebral Body Replacement (Oct 15, 2007)
- K050377: NBD Head Screw (Apr 7, 2005)
- K032196: NBD Disposable RF Cannulae (Oct 9, 2003)
- K021788: NBD Cement Restrictor Device (Oct 4, 2002)

Source page: https://510kreport.com/company/new-business-development