# Senecka Spine

- Location (FDA's records): Johnson City, NY
- FDA decisions: 2 (2015–2016): 2 510(k) clearances
- Product codes: NKB (2)
- Predicates its devices cite: 6 (1 its own); citations of its devices by later devices: 1 (1 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
- Scien'Tx USA, Inc.: 1 (https://510kreport.com/company/scien-tx-usa)
- K2m, Inc.: 1 (https://510kreport.com/company/k2m)
- Depuyacromed: 1 (https://510kreport.com/company/depuyacromed)
- U&I Corp., America: 1 (https://510kreport.com/company/u-i-america)
- Howmedica Osteonics Corp.: 1 (https://510kreport.com/company/howmedica-osteonics)

## Its most-cited devices
- K151849: Seneka I Polyscrew Pedicle Fixation System (2015), cited by 1

## Recent decisions
- K153525: Seneka II Polyscrew Pedicle Fixation System (Jan 28, 2016)
- K151849: Seneka I Polyscrew Pedicle Fixation System (Sep 30, 2015)

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