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FDA 510(k)

dS Small Extremity 16CH 1.5T Coil

K-Number: K162863 · 2016-11-07

Decision Date2016-11-07
Product CodeMOS
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

dS Small Extremity 16CH 1.5T Coil is the device name listed in this FDA 510(k) record. The listed applicant is Invivo Therapeutics Corporation. It received FDA 510(k) clearance on 2016-11-07 under 510(k) 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. The listed applicant is Invivo Therapeutics Corporation. The 510(k) number is K162863.

When did dS Small Extremity 16CH 1.5T Coil receive FDA 510(k) clearance?

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

Who is the listed applicant for dS Small Extremity 16CH 1.5T Coil?

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

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)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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.