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FDA 510(k)

Target Detachable Coils

K-Number: K242243 · 2024-08-29

ApplicantStryker Neurovscular
Decision Date2024-08-29
Product CodeHCG
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

Target Detachable Coils is a medical device manufactured by Stryker Neurovscular. It received FDA 510(k) clearance on 2024-08-29 under approval 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. It is manufactured by Stryker Neurovscular. The 510(k) number is K242243.

When was Target Detachable Coils approved by the FDA?

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

What company makes Target Detachable Coils?

Target Detachable Coils is manufactured by Stryker Neurovscular.

What is the FDA product code for Target Detachable Coils?

The FDA product code for Target Detachable Coils is HCG.

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Related Devices (Code: HCG)

K161367HydroCoil Embolic System (HES)MicroVention, Inc. K161452MicroPlex Coil System (MCS) - HyperSoft 3DMicroVention, Inc. K161429Target Detachable CoilsStryker Neurovascular K153658Target Detachable CoilsStryker Neurovascular K160832Penumbra Smart CoilPenumbra, Inc. K160096InZone Detachment SystemStryker Neurovascular

Official Source

View on FDA Database →

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

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