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FDA 510(k)

Intellijoint VIEW

K-Number: K211876 · 2021-11-12

Decision Date2021-11-12
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

Intellijoint VIEW is the device name listed in this FDA 510(k) record. The listed applicant is Intellijoint Surgical, Inc.. It received FDA 510(k) clearance on 2021-11-12 under 510(k) 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. The listed applicant is Intellijoint Surgical, Inc.. The 510(k) number is K211876.

When did Intellijoint VIEW receive FDA 510(k) clearance?

Intellijoint VIEW received FDA 510(k) clearance on 2021-11-12, under 510(k) number K211876.

Who is the listed applicant for Intellijoint VIEW?

The FDA 510(k) record lists Intellijoint Surgical, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Intellijoint VIEW?

The FDA product code for Intellijoint VIEW is LLZ.

Other records listing Intellijoint Surgical, Inc. 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: LLZ)

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

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