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FDA 510(k)

Instrument Clamps Electromagnetic

K-Number: K202609 · 2020-10-09

ApplicantStryker Corporation
Decision Date2020-10-09
Product CodePGW
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

Instrument Clamps Electromagnetic is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Corporation. It received FDA 510(k) clearance on 2020-10-09 under 510(k) number K202609. The device is classified under product code PGW. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Instrument Clamps Electromagnetic?

Instrument Clamps Electromagnetic is a medical device that received FDA 510(k) clearance on 2020-10-09. The listed applicant is Stryker Corporation. The 510(k) number is K202609.

When did Instrument Clamps Electromagnetic receive FDA 510(k) clearance?

Instrument Clamps Electromagnetic received FDA 510(k) clearance on 2020-10-09, under 510(k) number K202609.

Who is the listed applicant for Instrument Clamps Electromagnetic?

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

What is the FDA product code for Instrument Clamps Electromagnetic?

The FDA product code for Instrument Clamps Electromagnetic is PGW.

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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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