Libertas Taper Short (TS) Uncemented Femoral Stem (Libertas TS Stem)— 510(k) K253171
Substantially EquivalentMaxx Orthopedics, Inc.
FDA 510(k) clearance K253171 for Libertas Taper Short (TS) Uncemented Femoral Stem (Libertas TS Stem), Substantially Equivalent on 2026-01-15. Applicant: Maxx Orthopedics, Inc..
Clearance details
- Applicant
- Maxx Orthopedics, Inc.
- Product code
- Code LZO
- Advisory panel
- Orthopedic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Norristown, PA, US
Adverse events under product code LZO
product code LZO- Death
- 17
- Injury
- 12,942
- Malfunction
- 1,756
- Total
- 14,715
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Data sourced from openFDA. This site is unofficial and independent of the FDA.