Libertas Taper Uncemented Femoral Stem
K-Number: K183684 · 2019-08-23
Device Summary
Frequently Asked Questions
What is the Libertas Taper Uncemented Femoral Stem?
Libertas Taper Uncemented Femoral Stem is a medical device that received FDA 510(k) clearance on 2019-08-23. It is manufactured by Maxx Orthopedics, Inc.. The 510(k) number is K183684.
When was Libertas Taper Uncemented Femoral Stem approved by the FDA?
Libertas Taper Uncemented Femoral Stem received FDA 510(k) clearance on 2019-08-23, under approval number K183684.
What company makes Libertas Taper Uncemented Femoral Stem?
Libertas Taper Uncemented Femoral Stem is manufactured by Maxx Orthopedics, Inc..
What is the FDA product code for Libertas Taper Uncemented Femoral Stem?
The FDA product code for Libertas Taper Uncemented Femoral Stem is LZO.
Other Devices by Maxx Orthopedics, Inc.
Related Devices (Code: LZO)
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.