# K061461: Mayo Conservative Hip Prosthesis, Model 00.65-8026-010-05

- Pathway: 510(k) (Special)
- Applicant: Zimmer, Inc.
- Decided: Dec 20, 2006 after 208 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
Longest line of descent: 4 generations back to K850055 (1985). 15 ancestors in all.
5 later devices descend from it; 2 cite it directly.
0 of 20 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K030733: Mayo Conservative Hip Prosthesis, Model 8026 Series, Zimmer, Inc. (2003) Summary page 1.

## Most influential descendants
- K112682: Metha Hip System (2012), 2 descendants of its own
- K140547: Excera Fitrite Total Hip Arthroplasty System (2015), 1 descendant of its own
- K121684: Novation Lpi Prime Femoral Stem (2012), 1 descendant of its own
- K153057: FitRite™ Total Hip Arthroplasty System (2016), 0 descendants of its own
- K141821: Alteon Neck Preserving Femoral Stem, Standard Offset, Size 6-7; Alteon Neck Preserving Femoral Stem, Extended Offset (2014), 0 descendants of its own

## Indications for use
The MAYO Conservative Hip Prosthesis is indicated for cementless use in skeletally mature individuals undergoing primary surgery for total hip replacement. Diagnostic indications include severe hip pain and disabilities due to rheumatoid arthritis, osteoarthritis, traumatic arthritis, polyarthritis, slipped capital fernoral epiphysis, fused hip, fracture of the pelvis, and diastrophic variant.

Source page: https://510kreport.com/device/K061461
Methodology: https://510kreport.com/methodology