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FDA 510(k)

DePuy CONDUIT LLIF SQUID Inserter

K-Number: K220449 · 2022-06-28

ApplicantEnztec Limited
Decision Date2022-06-28
Product CodeMAX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

DePuy CONDUIT LLIF SQUID Inserter is the device name listed in this FDA 510(k) record. The listed applicant is Enztec Limited. It received FDA 510(k) clearance on 2022-06-28 under 510(k) number K220449. The device is classified under product code MAX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DePuy CONDUIT LLIF SQUID Inserter?

DePuy CONDUIT LLIF SQUID Inserter is a medical device that received FDA 510(k) clearance on 2022-06-28. The listed applicant is Enztec Limited. The 510(k) number is K220449.

When did DePuy CONDUIT LLIF SQUID Inserter receive FDA 510(k) clearance?

DePuy CONDUIT LLIF SQUID Inserter received FDA 510(k) clearance on 2022-06-28, under 510(k) number K220449.

Who is the listed applicant for DePuy CONDUIT LLIF SQUID Inserter?

The FDA 510(k) record lists Enztec Limited as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DePuy CONDUIT LLIF SQUID Inserter?

The FDA product code for DePuy CONDUIT LLIF SQUID Inserter is MAX.

Other records listing Enztec Limited 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.

K232014CONDUIT™ ATP InsertersK230876RI.KNEE Adjustable Tibia Cut GuideK223671CONDUIT LLIF Straight InsertersK212823DePuy CONDUIT LLIF Angled Inserters

Related Devices (Code: MAX)

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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