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FDA 510(k)

ADJUST-RIGHT FIXATION DEVICES

K-Number: K062734 · 2006-11-22

Decision Date2006-11-22
Product CodeJDR
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ADJUST-RIGHT FIXATION DEVICES is the device name listed in this FDA 510(k) record. The listed applicant is Valpo Orthopedic Technology, Inc.. It received FDA 510(k) clearance on 2006-11-22 under 510(k) number K062734. The device is classified under product code JDR. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ADJUST-RIGHT FIXATION DEVICES?

ADJUST-RIGHT FIXATION DEVICES is a medical device that received FDA 510(k) clearance on 2006-11-22. The listed applicant is Valpo Orthopedic Technology, Inc.. The 510(k) number is K062734.

When did ADJUST-RIGHT FIXATION DEVICES receive FDA 510(k) clearance?

ADJUST-RIGHT FIXATION DEVICES received FDA 510(k) clearance on 2006-11-22, under 510(k) number K062734.

Who is the listed applicant for ADJUST-RIGHT FIXATION DEVICES?

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

What is the FDA product code for ADJUST-RIGHT FIXATION DEVICES?

The FDA product code for ADJUST-RIGHT FIXATION DEVICES is JDR.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Valpo Orthopedic Technology, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Related Devices (Code: JDR)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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