Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

AMF Revision TT Cones

K-Number: K200653 · 2020-05-07

ApplicantLima Corporate S.P.A.
Decision Date2020-05-07
Product CodeJWH
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

AMF Revision TT Cones is a medical device manufactured by Lima Corporate S.P.A.. It received FDA 510(k) clearance on 2020-05-07 under approval number K200653. The device is classified under product code JWH. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AMF Revision TT Cones?

AMF Revision TT Cones is a medical device that received FDA 510(k) clearance on 2020-05-07. It is manufactured by Lima Corporate S.P.A.. The 510(k) number is K200653.

When was AMF Revision TT Cones approved by the FDA?

AMF Revision TT Cones received FDA 510(k) clearance on 2020-05-07, under approval number K200653.

What company makes AMF Revision TT Cones?

AMF Revision TT Cones is manufactured by Lima Corporate S.P.A..

What is the FDA product code for AMF Revision TT Cones?

The FDA product code for AMF Revision TT Cones is JWH.

Other Devices by Lima Corporate S.P.A.

K160011H-Max S stem K161476SMR Shoulder System K153722SMR 3-Pegs Glenoids K170473C2 femoral stem K163397SMR Hybrid Glenoid System K161120SMR TT Metal Back Glenoid, Bone Graft instruments

View all 41 devices →

Related Devices (Code: JWH)

K160515PS2 Knee SystemConsensus Orthopedics, Inc. K160771Destiknee Total Knee SystemMeril Healthcare Private Limited K160157LOSPA Modular Knee SystemCorentec Co., Ltd. K162273Materialise TKA Guide SystemMaterialise NV K162422Klassic Knee SystemTotal Joint Orthopedics, Inc. K161945EXPRT Revision Knee Femoral Augment(5mm), EXPRT Revision Knee Stem Extension (40mm)Encore Medical L.P.

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.

↑