# K955739: Modular Acetabular Shell II

- Pathway: 510(k) (Traditional)
- Applicant: Intermedics Orthopedics
- Decided: Mar 27, 1996 after 100 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 its predicate without a number.
- (no number) Option Shell: named in the summary without a submission number
- (no number) Acetabular Dome and Screw Hole Plugs: named in the summary without a submission number
- (no number) APR® Acetabular Shell: named in the summary without a submission number
- (no number) Non-Holed design of the Trilogy Acetabular System: named in the summary without a submission number

Source page: https://510kreport.com/device/K955739
Methodology: https://510kreport.com/methodology