Provata Implant System
K-Number: K222457 · 2023-03-06
Device Summary
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. The listed applicant is Southern Implants (Pty), Ltd.. The 510(k) number is K222457.
When did Provata Implant System receive FDA 510(k) clearance?
Provata Implant System received FDA 510(k) clearance on 2023-03-06, under 510(k) number K222457.
Who is the listed applicant for Provata Implant System?
The FDA 510(k) record lists Southern Implants (Pty), Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Provata Implant System?
The FDA product code for Provata Implant System is DZE.
Other records listing Southern Implants (Pty), Ltd. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: DZE)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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.