FDA 510(k)

Target Xtra Detachable Coil

K-Number: K261772 · 2026-06-24

Decision Date2026-06-24

Product CodeHCG

Advisory CommitteeNE

DecisionSubstantially Equivalent

Device Summary

Target Xtra Detachable Coil is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Neurovscular. It received FDA 510(k) clearance on 2026-06-24 under 510(k) number K261772. 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 Xtra Detachable Coil?

Target Xtra Detachable Coil is a medical device that received FDA 510(k) clearance on 2026-06-24. The listed applicant is Stryker Neurovscular. The 510(k) number is K261772.

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

Target Xtra Detachable Coil received FDA 510(k) clearance on 2026-06-24, under 510(k) number K261772.

Who is the listed applicant for Target Xtra Detachable Coil?

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 Xtra Detachable Coil?

The FDA product code for Target Xtra Detachable Coil is HCG.

Related Clinical Trials

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Other records listing Stryker Neurovscular as applicant

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Related Devices (Code: HCG)

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.