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FDA 510(k)

START JUNIOR

K-Number: K073512 · 2008-01-14

ApplicantOtto Bock Healthcare LP
Decision Date2008-01-14
Product CodeIOR
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

START JUNIOR is the device name listed in this FDA 510(k) record. The listed applicant is Otto Bock Healthcare LP. It received FDA 510(k) clearance on 2008-01-14 under 510(k) number K073512. The device is classified under product code IOR. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the START JUNIOR?

START JUNIOR is a medical device that received FDA 510(k) clearance on 2008-01-14. The listed applicant is Otto Bock Healthcare LP. The 510(k) number is K073512.

When did START JUNIOR receive FDA 510(k) clearance?

START JUNIOR received FDA 510(k) clearance on 2008-01-14, under 510(k) number K073512.

Who is the listed applicant for START JUNIOR?

The FDA 510(k) record lists Otto Bock Healthcare LP as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for START JUNIOR?

The FDA product code for START JUNIOR is IOR.

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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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