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FDA 510(k)

Provata Implant System

K-Number: K222457 · 2023-03-06

ApplicantSouthern Implants (Pty), Ltd.
Decision Date2023-03-06
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

Provata Implant System is a medical device manufactured by Southern Implants (Pty), Ltd.. It received FDA 510(k) clearance on 2023-03-06 under approval number K222457. The device is classified under product code DZE. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Provata Implant System?

Provata Implant System is a medical device that received FDA 510(k) clearance on 2023-03-06. It is manufactured by Southern Implants (Pty), Ltd.. The 510(k) number is K222457.

When was Provata Implant System approved by the FDA?

Provata Implant System received FDA 510(k) clearance on 2023-03-06, under approval number K222457.

What company makes Provata Implant System?

Provata Implant System is manufactured by Southern Implants (Pty), Ltd..

What is the FDA product code for Provata Implant System?

The FDA product code for Provata Implant System is DZE.

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Related PubMed Literature

PMID: 39892748 Long-term Safety and Performance of a Suprachoroidal Pressure Sensor System: Results of the EYEMATE-SC Trial Follow-up Study. Ophthalmology (2025) PMID: 41966145 From Registry to Reality: Opportunities to Enhance Post-market Surveillance of High-Risk Medical Devices Comment on "Quality and Utility of European Cardiovascular and Orthopaedic Registries for the Regulatory Evaluation of Medical Device Safety and Performance Across the Implant Lifecycle: A Systematic Review". International journal of health policy and management (2025) PMID: 39726899 How to improve the mechanical safety of a novel spinal implant while saving costs and time. JOR spine (2024)

Other Devices by Southern Implants (Pty), Ltd.

K161548Osseointegrated Fixtures K163634External Hex Implants K163060Deep Conical (DC) Implants and Accessories K181850Inversa Implants K180465Provata Implant System K173706Piccolo Implants and Accessories

View all 19 devices →

Related Devices (Code: DZE)

K160475Ritter Dental Implant SystemRitter Implants GmbH & Co. KG K161244s-Clean OneQ-SL Narrow Implant SystemDentis Co., Ltd. K163043Zeramex P6 Dental Implant SystemDentalpoint AG K161497Dental Implants and AbutmentsDitron Precision, Ltd. K153332ETIII SA Fixture System (O3.2mm)Hiossen, Inc. K151970KJ Mini Implant SystemKj Meditech Co., Ltd.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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