Intellijoint VIEW
K-Number: K211876 · 2021-11-12
ApplicantIntellijoint Surgical, Inc.
Decision Date2021-11-12
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
Intellijoint VIEW is a medical device manufactured by Intellijoint Surgical, Inc.. It received FDA 510(k) clearance on 2021-11-12 under approval number K211876. 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 Intellijoint VIEW?
Intellijoint VIEW is a medical device that received FDA 510(k) clearance on 2021-11-12. It is manufactured by Intellijoint Surgical, Inc.. The 510(k) number is K211876.
When was Intellijoint VIEW approved by the FDA?
Intellijoint VIEW received FDA 510(k) clearance on 2021-11-12, under approval number K211876.
What company makes Intellijoint VIEW?
Intellijoint VIEW is manufactured by Intellijoint Surgical, Inc..
What is the FDA product code for Intellijoint VIEW?
The FDA product code for Intellijoint VIEW is LLZ.
Other Devices by Intellijoint Surgical, Inc.
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.