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FDA 510(k)

POWER ADAPTOR INSTRUMENT ACCESSORY

K-Number: K120434 · 2012-03-08

ApplicantStryker Corp.
Decision Date2012-03-08
Product CodeNKB
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

POWER ADAPTOR INSTRUMENT ACCESSORY is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Corp.. It received FDA 510(k) clearance on 2012-03-08 under 510(k) number K120434. 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 POWER ADAPTOR INSTRUMENT ACCESSORY?

POWER ADAPTOR INSTRUMENT ACCESSORY is a medical device that received FDA 510(k) clearance on 2012-03-08. The listed applicant is Stryker Corp.. The 510(k) number is K120434.

When did POWER ADAPTOR INSTRUMENT ACCESSORY receive FDA 510(k) clearance?

POWER ADAPTOR INSTRUMENT ACCESSORY received FDA 510(k) clearance on 2012-03-08, under 510(k) number K120434.

Who is the listed applicant for POWER ADAPTOR INSTRUMENT ACCESSORY?

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

What is the FDA product code for POWER ADAPTOR INSTRUMENT ACCESSORY?

The FDA product code for POWER ADAPTOR INSTRUMENT ACCESSORY is NKB.

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Related Devices (Code: 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.

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