# K030153: Zca All-Poly Acetabular Cup, Snap-in, Model 8005-946/958-32

- Pathway: 510(k) (Traditional)
- Applicant: Zimmer, Inc.
- Decided: Apr 1, 2003 after 75 days
- Product code: JDI (Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented)
- Device class: 2
- Regulation: 21 CFR 888.3350
- 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 K901240 (1990). 3 ancestors in all.
17 later devices descend from it; 3 cite it directly.
0 of 21 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K901240: Astel Non-Metal Backed Acetabular Cup for Cemented, Med-Tek Corp. (1990) Summary page 1.
- K924115: Ultima All Uhmwpe Cemented Acetabular Cups, Johnson & Johnson Orthopaedics, Inc. (1992) Summary page 1.
- K934765: Trilogy Acetabular System, Zimmer, Inc. (1994) Summary page 1.
- (no number) Trapezoidal-28 Snap-On Acetabular Cup: named in the summary without a submission number
- (no number) Müller Snap-On Acetabular Cup: named in the summary without a submission number

## Most influential descendants
- K112158: Modulus Stems, Modulus Necks, Modular Femoral Heads, Cemented Cups, Lock Bipolar Heads (2012), 13 descendants of its own
- K141327: Minima S System (2014), 5 descendants of its own
- K152903: REVIVAL (TM) Modular Revision Hip Stem (2016), 4 descendants of its own
- K140975: Mastersl Femoral Stem (2014), 4 descendants of its own
- K191374: Revival Modular Hip Stem (2019), 3 descendants of its own

## Indications for use
The acetabular cup is intended for cemented use in skeletally mature individuals undergoing primary or revision surgery for rehabilitating hips damaged as a result of noninflammatory degenerative joint disease (NIDJD) or its composite diagnoses of osteoarthritis, avascular necrosis, traumatic arthritis, slipped capital epiphysis, fused hip, fracture of the pelvis, and diastrophic variant.

Source page: https://510kreport.com/device/K030153
Methodology: https://510kreport.com/methodology