# K070050: Vitality Hip System Model#420

- Pathway: 510(k) (Traditional)
- Applicant: Encore Medical L.P.
- Decided: May 23, 2007 after 139 days
- Product code: LPH (Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented)
- Device class: 2
- Regulation: 21 CFR 888.3358
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names no predicate by number.

## Indications for use
Joint replacement is indicated for patients suffering from disability due to: * noninflammatory degenerative joint disease including osteoarthritis and avascular necrosis of the natural femoral head; * rheumatoid arthritis; * correction of functional deformity; * femoral fracture This device may also be indicated in the salvage of previously failed surgical attempts. The Encore hip systems are for total hip replacement except for the bipolar or unipolar hip systems which are for hemi-afftroplasty applications. The CLP Offset, CLP-R, and Stamina hip systems are for either total or hemi-applications. The following Hip Systems are for Cementless application: Linear Stamina Keystone Modular Revelation Foundation Press-Fit CLP Offset CLP I Foundation Fracture The following hip systems are for cemented application: Vitality Foundation Cemented The following hip systems are for either cemented or cementless applications: Alpha Il CLP R R120 R12OPC

Source page: https://510kreport.com/device/K070050
Methodology: https://510kreport.com/methodology