# K955137: IM C-Ment Acetabular Cap

- Pathway: 510(k) (Traditional)
- Applicant: Implant Ideas, LLC
- Decided: Oct 10, 1996 after 332 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
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) M.E. Muller Type Acetabular Cups from DePuy: named in the summary without a submission number
- (no number) Charnley Type Acetabular Cup from DePuy: named in the summary without a submission number
- (no number) New England Baptist Hip Cups from DePuy: named in the summary without a submission number

## Indications for use
The IM C-Ment Acetabular Cup will be used in indications which are the same as that for other acetabular components of cemented total hip replacement systems. Specifically, the IM C-Ment Acetabular Cup is intended to resurface the acetabular socket in cases of femoral head and neck fractures, nonunion of femoral head and neck fractures, femoral head aseptic necrosis, osteoarthritis, rheumatoid arthritis and revision of failed prostheses. The IM C-Ment Acetabular Cup is intended to be used in cemented applications only.

Source page: https://510kreport.com/device/K955137
Methodology: https://510kreport.com/methodology