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FDA 510(k)

Sherlock

K-Number: K212664 · 2021-11-30

Decision Date2021-11-30
Product CodeNHA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

Sherlock is the device name listed in this FDA 510(k) record. The listed applicant is Open Implants, LLC. It received FDA 510(k) clearance on 2021-11-30 under 510(k) number K212664. The device is classified under product code NHA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Sherlock?

Sherlock is a medical device that received FDA 510(k) clearance on 2021-11-30. The listed applicant is Open Implants, LLC. The 510(k) number is K212664.

When did Sherlock receive FDA 510(k) clearance?

Sherlock received FDA 510(k) clearance on 2021-11-30, under 510(k) number K212664.

Who is the listed applicant for Sherlock?

The FDA 510(k) record lists Open Implants, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Sherlock?

The FDA product code for Sherlock is NHA.

Other records listing Open Implants, LLC 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: NHA)

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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