FDA 510(k)

dS Small Extremity 16CH 1.5T Coil

K-Number: K162863 · 2016-11-07

ApplicantInvivo Therapeutics Corporation

Decision Date2016-11-07

Product CodeMOS

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

dS Small Extremity 16CH 1.5T Coil is a medical device manufactured by Invivo Therapeutics Corporation. It received FDA 510(k) clearance on 2016-11-07 under approval number K162863. The device is classified under product code MOS. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the dS Small Extremity 16CH 1.5T Coil?

dS Small Extremity 16CH 1.5T Coil is a medical device that received FDA 510(k) clearance on 2016-11-07. It is manufactured by Invivo Therapeutics Corporation. The 510(k) number is K162863.

When was dS Small Extremity 16CH 1.5T Coil approved by the FDA?

dS Small Extremity 16CH 1.5T Coil received FDA 510(k) clearance on 2016-11-07, under approval number K162863.

What company makes dS Small Extremity 16CH 1.5T Coil?

dS Small Extremity 16CH 1.5T Coil is manufactured by Invivo Therapeutics Corporation.

What is the FDA product code for dS Small Extremity 16CH 1.5T Coil?

The FDA product code for dS Small Extremity 16CH 1.5T Coil is MOS.

Related Devices (Code: MOS)

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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.