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FDA 510(k)

PIN SCREW

K-Number: K061599 · 2006-07-26

ApplicantBk Meditech, Co., Ltd.
Decision Date2006-07-26
Product CodeJDW
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

PIN SCREW is the device name listed in this FDA 510(k) record. The listed applicant is Bk Meditech, Co., Ltd.. It received FDA 510(k) clearance on 2006-07-26 under 510(k) number K061599. The device is classified under product code JDW. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PIN SCREW?

PIN SCREW is a medical device that received FDA 510(k) clearance on 2006-07-26. The listed applicant is Bk Meditech, Co., Ltd.. The 510(k) number is K061599.

When did PIN SCREW receive FDA 510(k) clearance?

PIN SCREW received FDA 510(k) clearance on 2006-07-26, under 510(k) number K061599.

Who is the listed applicant for PIN SCREW?

The FDA 510(k) record lists Bk Meditech, Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PIN SCREW?

The FDA product code for PIN SCREW is JDW.

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Related Devices (Code: JDW)

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

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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