FDA 510(k)

Target Detachable Coils

K-Number: K242243 · 2024-08-29

Decision Date2024-08-29

Product CodeHCG

Advisory CommitteeNE

DecisionSubstantially Equivalent

Device Summary

Target Detachable Coils is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Neurovscular. It received FDA 510(k) clearance on 2024-08-29 under 510(k) number K242243. The device is classified under product code HCG. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Target Detachable Coils?

Target Detachable Coils is a medical device that received FDA 510(k) clearance on 2024-08-29. The listed applicant is Stryker Neurovscular. The 510(k) number is K242243.

When did Target Detachable Coils receive FDA 510(k) clearance?

Target Detachable Coils received FDA 510(k) clearance on 2024-08-29, under 510(k) number K242243.

Who is the listed applicant for Target Detachable Coils?

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

What is the FDA product code for Target Detachable Coils?

The FDA product code for Target Detachable Coils is HCG.

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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.