MOTO PFJ System
K-Number: K200122 · 2020-04-20
ApplicantMedacta International S.A.
Decision Date2020-04-20
Product CodeKRR
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
MOTO PFJ System is a medical device manufactured by Medacta International S.A.. It received FDA 510(k) clearance on 2020-04-20 under approval number K200122. The device is classified under product code KRR. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the MOTO PFJ System?
MOTO PFJ System is a medical device that received FDA 510(k) clearance on 2020-04-20. It is manufactured by Medacta International S.A.. The 510(k) number is K200122.
When was MOTO PFJ System approved by the FDA?
MOTO PFJ System received FDA 510(k) clearance on 2020-04-20, under approval number K200122.
What company makes MOTO PFJ System?
MOTO PFJ System is manufactured by Medacta International S.A..
What is the FDA product code for MOTO PFJ System?
The FDA product code for MOTO PFJ System is KRR.
Other Devices by Medacta International S.A.
Related Devices (Code: KRR)
K160461Arthrex iBalance BiCompartmental Arthroplasty SystemArthrex, Inc.
K181280Patello-Femoral Wave (Kahuna) Arthroplasty SystemArthrosurface, Inc.
K211303Avon Patello-femoral Joint ProsthesisHowmedica Osteonics Corp., Dba Stryker Orthopaedics
K221048Episealer Patellofemoral SystemEpisurf Medical, Inc.
K231253Overture Orthopaedics Patellofemoral SystemOverture Resurfacing, 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.