# Intelivation, LLC

- Location (FDA's records): Saint Simons Island, GA
- FDA decisions: 3 (2021–2023): 3 510(k) clearances
- Names in FDA's records: Intelivation, LLC (2); Intelivation (1)
- Product codes: HTY (1), MAX (1), NKB (1)
- 510(k) review time since 2016: median 88 days, against 109 for FDA's reviews in the same codes and years (2 of 3 faster)
- Predicates its devices cite: 7 (0 its own); citations of its devices by later devices: 0 (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
- Accel Spine: 2 (https://510kreport.com/company/accel-spine)
- Arthrex, Inc.: 1 (https://510kreport.com/company/arthrex)
- Aap Implantate AG: 1 (https://510kreport.com/company/aap-implantate)
- Globus Medical, Inc.: 1 (https://510kreport.com/company/globus-medical)
- Jeil Medical Corporation: 1 (https://510kreport.com/company/jeil-medical)
- Amedica Corp.: 1 (https://510kreport.com/company/amedica)

## Recent decisions
- K231147: Hammerdesis™ Interphalangeal Fusion System (Sep 14, 2023)
- K212389: Advantage Lumbar System - ALIF, PLIF, DLIF, TLIF (Oct 29, 2021)
- K212185: Golden Isles Pedicle Screw System (Aug 19, 2021)

Source page: https://510kreport.com/company/intelivation