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FDA 510(k)

Cannulated Power Driver Attachment

K-Number: K202528 · 2020-10-26

ApplicantK2m, Inc.
Decision Date2020-10-26
Product CodeNKB
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Cannulated Power Driver Attachment is the device name listed in this FDA 510(k) record. The listed applicant is K2m, Inc.. It received FDA 510(k) clearance on 2020-10-26 under 510(k) number K202528. The device is classified under product code NKB. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Cannulated Power Driver Attachment?

Cannulated Power Driver Attachment is a medical device that received FDA 510(k) clearance on 2020-10-26. The listed applicant is K2m, Inc.. The 510(k) number is K202528.

When did Cannulated Power Driver Attachment receive FDA 510(k) clearance?

Cannulated Power Driver Attachment received FDA 510(k) clearance on 2020-10-26, under 510(k) number K202528.

Who is the listed applicant for Cannulated Power Driver Attachment?

The FDA 510(k) record lists K2m, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Cannulated Power Driver Attachment?

The FDA product code for Cannulated Power Driver Attachment is NKB.

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Related Devices (Code: NKB)

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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