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 a medical device manufactured by K2m, Inc.. It received FDA 510(k) clearance on 2020-10-26 under approval 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. It is manufactured by K2m, Inc.. The 510(k) number is K202528.
When was Cannulated Power Driver Attachment approved by the FDA?
Cannulated Power Driver Attachment received FDA 510(k) clearance on 2020-10-26, under approval number K202528.
What company makes Cannulated Power Driver Attachment?
Cannulated Power Driver Attachment is manufactured by K2m, Inc..
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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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.