# Elite Surgical Supplies (Pty), Ltd.

- Location (FDA's records): Marietta, GA
- FDA decisions: 4 (2007–2020): 4 510(k) clearances
- Product codes: MNI (2), KWQ (1), MAX (1)
- Predicates its devices cite: 7 (1 its own); citations of its devices by later devices: 3 (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
- U&I Corporation: 1 (https://510kreport.com/company/u-i)
- Blackstone Medical, Inc.: 1 (https://510kreport.com/company/blackstone-medical)
- Meditech Spine, LLC: 1 (https://510kreport.com/company/meditech-spine)
- Spinecraft, LLC: 1 (https://510kreport.com/company/spinecraft)
- Advanced Medical Technologies AG: 1 (https://510kreport.com/company/advanced-medical-technologies)
- Surgicraft, Ltd.: 1 (https://510kreport.com/company/surgicraft)

## Firms that cite its devices most
- Alliance Partners, LLC: 1 (https://510kreport.com/company/alliance-partners)
- Aesculap Implant Systems, LLC: 1 (https://510kreport.com/company/aesculap-implant-systems)

## Its most-cited devices
- K130274: Biolign Acif Systems, Biolign Stacc Acif System, Biolign Tlif System (2013), cited by 2
- K063453: Vertefix Pedicle Screw Spinal System (2007), cited by 1

## Recent decisions
- K200523: Biolign® Roto-Loc Cervical Plate System (Apr 30, 2020)
- K130274: Biolign Acif Systems, Biolign Stacc Acif System, Biolign Tlif System (Oct 29, 2013)
- K080075: Modification to: Vertefix Pedicle Screw Spinal System (Jan 28, 2008)
- K063453: Vertefix Pedicle Screw Spinal System (Aug 30, 2007)

Source page: https://510kreport.com/company/elite-surgical-supplies