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FDA 510(k)

CTL-63 AND CTL-128 SPINE ARRAY COILS

K-Number: K062767 · 2006-10-13

ApplicantInvivo Corporation
Decision Date2006-10-13
Product CodeMOS
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CTL-63 AND CTL-128 SPINE ARRAY COILS is the device name listed in this FDA 510(k) record. The listed applicant is Invivo Corporation. It received FDA 510(k) clearance on 2006-10-13 under 510(k) number K062767. 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 CTL-63 AND CTL-128 SPINE ARRAY COILS?

CTL-63 AND CTL-128 SPINE ARRAY COILS is a medical device that received FDA 510(k) clearance on 2006-10-13. The listed applicant is Invivo Corporation. The 510(k) number is K062767.

When did CTL-63 AND CTL-128 SPINE ARRAY COILS receive FDA 510(k) clearance?

CTL-63 AND CTL-128 SPINE ARRAY COILS received FDA 510(k) clearance on 2006-10-13, under 510(k) number K062767.

Who is the listed applicant for CTL-63 AND CTL-128 SPINE ARRAY COILS?

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

What is the FDA product code for CTL-63 AND CTL-128 SPINE ARRAY COILS?

The FDA product code for CTL-63 AND CTL-128 SPINE ARRAY COILS is MOS.

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Related Devices (Code: MOS)

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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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