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FDA 510(k)

GROWTH GUIDANCE PLATE

K-Number: K031493 · 2003-11-20

ApplicantUniversity of Utah/School of Medicine
Decision Date2003-11-20
Product CodeHRS
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

GROWTH GUIDANCE PLATE is the device name listed in this FDA 510(k) record. The listed applicant is University of Utah/School of Medicine. It received FDA 510(k) clearance on 2003-11-20 under 510(k) number K031493. The device is classified under product code HRS. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GROWTH GUIDANCE PLATE?

GROWTH GUIDANCE PLATE is a medical device that received FDA 510(k) clearance on 2003-11-20. The listed applicant is University of Utah/School of Medicine. The 510(k) number is K031493.

When did GROWTH GUIDANCE PLATE receive FDA 510(k) clearance?

GROWTH GUIDANCE PLATE received FDA 510(k) clearance on 2003-11-20, under 510(k) number K031493.

Who is the listed applicant for GROWTH GUIDANCE PLATE?

The FDA 510(k) record lists University of Utah/School of Medicine as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for GROWTH GUIDANCE PLATE?

The FDA product code for GROWTH GUIDANCE PLATE is HRS.

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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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