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FDA 510(k)

ORTHOCAD IQ

K-Number: K082207 · 2009-10-23

ApplicantCadent, Inc.
Decision Date2009-10-23
Product CodeDYW
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ORTHOCAD IQ is the device name listed in this FDA 510(k) record. The listed applicant is Cadent, Inc.. It received FDA 510(k) clearance on 2009-10-23 under 510(k) number K082207. The device is classified under product code DYW. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ORTHOCAD IQ?

ORTHOCAD IQ is a medical device that received FDA 510(k) clearance on 2009-10-23. The listed applicant is Cadent, Inc.. The 510(k) number is K082207.

When did ORTHOCAD IQ receive FDA 510(k) clearance?

ORTHOCAD IQ received FDA 510(k) clearance on 2009-10-23, under 510(k) number K082207.

Who is the listed applicant for ORTHOCAD IQ?

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

What is the FDA product code for ORTHOCAD IQ?

The FDA product code for ORTHOCAD IQ is DYW.

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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.

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