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FDA 510(k)

ZIPKNOT, MODEL 1017-3000

K-Number: K072525 · 2007-10-05

ApplicantMedicinelodge, Inc.
Decision Date2007-10-05
Product CodeFZP
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ZIPKNOT, MODEL 1017-3000 is the device name listed in this FDA 510(k) record. The listed applicant is Medicinelodge, Inc.. It received FDA 510(k) clearance on 2007-10-05 under 510(k) number K072525. The device is classified under product code FZP. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ZIPKNOT, MODEL 1017-3000?

ZIPKNOT, MODEL 1017-3000 is a medical device that received FDA 510(k) clearance on 2007-10-05. The listed applicant is Medicinelodge, Inc.. The 510(k) number is K072525.

When did ZIPKNOT, MODEL 1017-3000 receive FDA 510(k) clearance?

ZIPKNOT, MODEL 1017-3000 received FDA 510(k) clearance on 2007-10-05, under 510(k) number K072525.

Who is the listed applicant for ZIPKNOT, MODEL 1017-3000?

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 ZIPKNOT, MODEL 1017-3000?

The FDA product code for ZIPKNOT, MODEL 1017-3000 is FZP.

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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.

K051488MEDICINELODGE ZIPKNOTK962705MLI MODULAR STAPLEK961920CROSS PINK961905MEDICINELODGE, INC. SET SCREWK962194MLI SOFT TISSUE SCREW & WASHER SYSTEMK961025EXPANDED BODY SUTURE

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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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