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FDA 510(k)

Remanufactured EndoWrist ProGrasp Forceps (420093)

K-Number: K241872 · 2024-11-07

ApplicantRebotix
Decision Date2024-11-07
Product CodeQSM
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

Remanufactured EndoWrist ProGrasp Forceps (420093) is a medical device manufactured by Rebotix. It received FDA 510(k) clearance on 2024-11-07 under approval number K241872. The device is classified under product code QSM. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Remanufactured EndoWrist ProGrasp Forceps (420093)?

Remanufactured EndoWrist ProGrasp Forceps (420093) is a medical device that received FDA 510(k) clearance on 2024-11-07. It is manufactured by Rebotix. The 510(k) number is K241872.

When was Remanufactured EndoWrist ProGrasp Forceps (420093) approved by the FDA?

Remanufactured EndoWrist ProGrasp Forceps (420093) received FDA 510(k) clearance on 2024-11-07, under approval number K241872.

What company makes Remanufactured EndoWrist ProGrasp Forceps (420093)?

Remanufactured EndoWrist ProGrasp Forceps (420093) is manufactured by Rebotix.

What is the FDA product code for Remanufactured EndoWrist ProGrasp Forceps (420093)?

The FDA product code for Remanufactured EndoWrist ProGrasp Forceps (420093) is QSM.

Other Devices by Rebotix

K250417Remanufactured EndoWrist Cobra Grasper (420190) K250387Remanufactured EndoWrist Long Tip Forceps (420048) K250399Remanufactured EndoWrist Cadiere Forceps (420049) K250539Remanufactured EndoWrist Tenaculum Forceps (420207)

Related Devices (Code: QSM)

K2104788mm Monopolar Curved ScissorsIconocare Health K250417Remanufactured EndoWrist Cobra Grasper (420190)Rebotix K250387Remanufactured EndoWrist Long Tip Forceps (420048)Rebotix K250399Remanufactured EndoWrist Cadiere Forceps (420049)Rebotix K250539Remanufactured EndoWrist Tenaculum Forceps (420207)Rebotix K2426108mm Monopolar Curved Scissors (470179)Iconocare Health

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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