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)

FMP Extended Liners

K-Number: K172651 · 2017-12-13

ApplicantEncore Medical L.P.
Decision Date2017-12-13
Product CodeOQG
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

FMP Extended Liners is a medical device manufactured by Encore Medical L.P.. It received FDA 510(k) clearance on 2017-12-13 under approval number K172651. The device is classified under product code OQG. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FMP Extended Liners?

FMP Extended Liners is a medical device that received FDA 510(k) clearance on 2017-12-13. It is manufactured by Encore Medical L.P.. The 510(k) number is K172651.

When was FMP Extended Liners approved by the FDA?

FMP Extended Liners received FDA 510(k) clearance on 2017-12-13, under approval number K172651.

What company makes FMP Extended Liners?

FMP Extended Liners is manufactured by Encore Medical L.P..

What is the FDA product code for FMP Extended Liners?

The FDA product code for FMP Extended Liners is OQG.

Other Devices by Encore Medical L.P.

K162024AltiVate Anatomic Shoulder System K161610EXPRT Revision Hip System K161945EXPRT Revision Knee Femoral Augment(5mm), EXPRT Revision Knee Stem Extension (40mm) K160342EMPOWR PS Knee System K173073AltiVate Anatomic to Reverse Conversion Module K172351AltiVate Reverse Humeral Stem, AltiVate Reverse Small Spacer, Altivate Reverse, Small Hemi-Adapter, AltiVate Reverse, Small Socket Insert

View all 31 devices →

Related Devices (Code: OQG)

K171543Renovis Surgical Hip Replacement SystemRenovis Surgical Technologies K173104Klassic HD® Hooded Acetabular Insert with E-Link® Poly, Klassic HD® Low Profile Acetabular Insert with E-Link® PolyTotal Joint Orthopedics, Inc. K201660KMTI Hip Replacement System, Tesera Trabecular Technologies (T3) Acetabular Shell System, Porous Acetabular Cup SystemKyocera Medical Technologies, Inc. K200328Tesera Trabecular Technologies (T3) Acetabular Shell System, Porous Acetabular Cup SystemKyocera Medical Technologies, Inc. K202705Prime and DYNASTY® Additive Manufacturing ShellsMicroport Orthopedics, Inc. K203472KMTI Hip Replacement SystemKyocera Medical Technologies, 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.

↑