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 a medical device manufactured by Stryker Corporation. It received FDA 510(k) clearance on 2020-10-09 under approval 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. It is manufactured by Stryker Corporation. The 510(k) number is K202609.
When was Instrument Clamps Electromagnetic approved by the FDA?
Instrument Clamps Electromagnetic received FDA 510(k) clearance on 2020-10-09, under approval number K202609.
What company makes Instrument Clamps Electromagnetic?
Instrument Clamps Electromagnetic is manufactured by Stryker Corporation.
What is the FDA product code for Instrument Clamps Electromagnetic?
The FDA product code for Instrument Clamps Electromagnetic is PGW.
Other Devices by Stryker Corporation
Related Devices (Code: PGW)
K162176Fiagon Navigation SystemFiagon GmbH
K161697Acclarent NavWire Sinus Navigation GuidewireAcclarent, Inc.
K161701CARTO ENT SystemBiosense Webster
K161555KARL STORZ NAV1 Electromagnetic Navigation SystemKarl Storz Endoscopy America, Inc.
K161940Guidewire 0.6 Single UseFiagon GmbH
K153555EM ENT Navigated SuctionsMedtronic Navigation, Inc.
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.