# K073068: Accin Hip System

- Pathway: 510(k) (Traditional)
- Applicant: Accelerated Innovation, LLC
- Decided: Jan 10, 2008 after 72 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: 1 generation back to K934162 (1994). 7 ancestors in all.
28 later devices descend from it; 3 cite it directly.
0 of 36 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K935484: Provident Hip System, Stelkast Company (1994) Summary page 1.
- K946371: Provident HP System, Stelkast Company (1995) Summary page 1.
- K960180: 22 MM Cocr Head & Polyethlene Liner, Stelkast Company (1996) Summary page 1.
- K991622: 26 MM Cast Cocr Head and Polyethylene Acetabular Shell Liner, Stelkast Company (1999) Summary page 1.
- K001745: Modification to Provident Hip System, Stelkast Company (2000) Summary page 1.
- K002796: Modification to Provident Hip System, Stelkast Company (2000) Summary page 1.
- K934162: Proform HA Hip System, Stelkast Company (1994) Summary page 1.

## Most influential descendants
- K100445: Klassic HD Hip System (2010), 25 descendants of its own
- K143407: Klassic HD Hip System (2014), 16 descendants of its own
- K141972: Klassic HD Acetabular Insert with E-Link Poly (2014), 14 descendants of its own
- K163577: Ecofit® Hip System (2017), 9 descendants of its own
- K173104: Klassic HD® Hooded Acetabular Insert with E-Link® Poly, Klassic HD® Low Profile Acetabular Insert with E-Link® Poly (2017), 6 descendants of its own

## Indications for use
The AccinTM Hip System components are for use in total hip arthroplasty as a result of: * Hip arthritis caused by rheumatoid disease, non-inflammatory degenerative joint disease, osteoarthritis and arthritis resulting from biologic or mechanical trauma to the hip * Correction of functional deformity * Avascular necrosis * Treatment of non-unions, femoral neck and trochanteric fractures of the proximal femur * Difficult clinical management problems involving persistent pain and physical impairment where conventional arthodesis is not likely to achieve satisfactory results. These components are single use only and are intended for implantation without bone cement.

Source page: https://510kreport.com/device/K073068
Methodology: https://510kreport.com/methodology