Remanufactured EndoWrist ProGrasp Forceps (420093)
K-Number: K241872 · 2024-11-07
Device Summary
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. The listed applicant is Rebotix. The 510(k) number is K241872.
When did Remanufactured EndoWrist ProGrasp Forceps (420093) receive FDA 510(k) clearance?
Remanufactured EndoWrist ProGrasp Forceps (420093) received FDA 510(k) clearance on 2024-11-07, under 510(k) number K241872.
Who is the listed applicant for Remanufactured EndoWrist ProGrasp Forceps (420093)?
The FDA 510(k) record lists Rebotix as the applicant. This does not by itself establish the device manufacturer.
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 records listing Rebotix as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: QSM)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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.