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FDA 510(k)

Libertas Taper Short (TS) Uncemented Femoral Stem (Libertas TS Stem)

K-Number: K253171 · 2026-01-15

Decision Date2026-01-15
Product CodeLZO
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Libertas Taper Short (TS) Uncemented Femoral Stem (Libertas TS Stem) is a medical device manufactured by Maxx Orthopedics, Inc.. It received FDA 510(k) clearance on 2026-01-15 under approval number K253171. 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 Short (TS) Uncemented Femoral Stem (Libertas TS Stem)?

Libertas Taper Short (TS) Uncemented Femoral Stem (Libertas TS Stem) is a medical device that received FDA 510(k) clearance on 2026-01-15. It is manufactured by Maxx Orthopedics, Inc.. The 510(k) number is K253171.

When was Libertas Taper Short (TS) Uncemented Femoral Stem (Libertas TS Stem) approved by the FDA?

Libertas Taper Short (TS) Uncemented Femoral Stem (Libertas TS Stem) received FDA 510(k) clearance on 2026-01-15, under approval number K253171.

What company makes Libertas Taper Short (TS) Uncemented Femoral Stem (Libertas TS Stem)?

Libertas Taper Short (TS) Uncemented Femoral Stem (Libertas TS Stem) is manufactured by Maxx Orthopedics, Inc..

What is the FDA product code for Libertas Taper Short (TS) Uncemented Femoral Stem (Libertas TS Stem)?

The FDA product code for Libertas Taper Short (TS) Uncemented Femoral Stem (Libertas TS Stem) is LZO.

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Official Source

View on FDA Database →

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