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FDA 510(k)

MEDICINELODGE ZIPKNOT

K-Number: K051488 · 2005-07-27

Decision Date2005-07-27
Product CodeNVH
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MEDICINELODGE ZIPKNOT is the device name listed in this FDA 510(k) record. The listed applicant is Medicinelodge, Inc.. It received FDA 510(k) clearance on 2005-07-27 under 510(k) number K051488. The device is classified under product code NVH. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDICINELODGE ZIPKNOT?

MEDICINELODGE ZIPKNOT is a medical device that received FDA 510(k) clearance on 2005-07-27. The listed applicant is Medicinelodge, Inc.. The 510(k) number is K051488.

When did MEDICINELODGE ZIPKNOT receive FDA 510(k) clearance?

MEDICINELODGE ZIPKNOT received FDA 510(k) clearance on 2005-07-27, under 510(k) number K051488.

Who is the listed applicant for MEDICINELODGE ZIPKNOT?

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

What is the FDA product code for MEDICINELODGE ZIPKNOT?

The FDA product code for MEDICINELODGE ZIPKNOT is NVH.

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 Medicinelodge, 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.

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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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