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FDA 510(k)

Libertas – Taper Uncemented Femoral Stem

K-Number: K183684 · 2019-08-23

Decision Date2019-08-23
Product CodeLZO
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Libertas – Taper Uncemented Femoral Stem is a medical device manufactured by Maxx Orthopedics, Inc.. It received FDA 510(k) clearance on 2019-08-23 under approval number K183684. The device is classified under product code LZO. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

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.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.