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FDA 510(k)

KIT MENDEC SPINE AND DELIVERY SYSTEM

K-Number: K062452 · 2006-09-21

ApplicantTecres S.P.A.
Decision Date2006-09-21
Product CodeNDN
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

KIT MENDEC SPINE AND DELIVERY SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Tecres S.P.A.. It received FDA 510(k) clearance on 2006-09-21 under 510(k) number K062452. The device is classified under product code NDN. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KIT MENDEC SPINE AND DELIVERY SYSTEM?

KIT MENDEC SPINE AND DELIVERY SYSTEM is a medical device that received FDA 510(k) clearance on 2006-09-21. The listed applicant is Tecres S.P.A.. The 510(k) number is K062452.

When did KIT MENDEC SPINE AND DELIVERY SYSTEM receive FDA 510(k) clearance?

KIT MENDEC SPINE AND DELIVERY SYSTEM received FDA 510(k) clearance on 2006-09-21, under 510(k) number K062452.

Who is the listed applicant for KIT MENDEC SPINE AND DELIVERY SYSTEM?

The FDA 510(k) record lists Tecres S.P.A. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for KIT MENDEC SPINE AND DELIVERY SYSTEM?

The FDA product code for KIT MENDEC SPINE AND DELIVERY SYSTEM is NDN.

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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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