ImplaStation
K-Number: K210241 · 2021-12-03
ApplicantProdigident, Inc.
Decision Date2021-12-03
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
ImplaStation is a medical device manufactured by Prodigident, Inc.. It received FDA 510(k) clearance on 2021-12-03 under approval number K210241. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the ImplaStation?
ImplaStation is a medical device that received FDA 510(k) clearance on 2021-12-03. It is manufactured by Prodigident, Inc.. The 510(k) number is K210241.
When was ImplaStation approved by the FDA?
ImplaStation received FDA 510(k) clearance on 2021-12-03, under approval number K210241.
What company makes ImplaStation?
ImplaStation is manufactured by Prodigident, Inc..
What is the FDA product code for ImplaStation?
The FDA product code for ImplaStation is LLZ.
Related Devices (Code: LLZ)
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.