Target Detachable Coils
K-Number: K161429 · 2016-06-22
ApplicantStryker Neurovascular
Decision Date2016-06-22
Product CodeHCG
Advisory CommitteeNE
DecisionSubstantially Equivalent
Device Summary
Target Detachable Coils is a medical device manufactured by Stryker Neurovascular. It received FDA 510(k) clearance on 2016-06-22 under approval number K161429. 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 2016-06-22. It is manufactured by Stryker Neurovascular. The 510(k) number is K161429.
When was Target Detachable Coils approved by the FDA?
Target Detachable Coils received FDA 510(k) clearance on 2016-06-22, under approval number K161429.
What company makes Target Detachable Coils?
Target Detachable Coils is manufactured by Stryker Neurovascular.
What is the FDA product code for Target Detachable Coils?
The FDA product code for Target Detachable Coils is HCG.
Related Clinical Trials
Other Devices by Stryker Neurovascular
Related Devices (Code: HCG)
K161367HydroCoil Embolic System (HES)MicroVention, Inc.
K161452MicroPlex Coil System (MCS) - HyperSoft 3DMicroVention, Inc.
K153658Target Detachable CoilsStryker Neurovascular
K160832Penumbra Smart CoilPenumbra, Inc.
K160096InZone Detachment SystemStryker Neurovascular
K153594MicroPlex Coil System (MCS), Hydrocoil Embolic System (HES)MicroVention, Inc.
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.