# K101582: Cam Structsure Bars

- Pathway: 510(k) (Special)
- Applicant: Biomet 3i, Inc.
- Decided: Nov 8, 2010 after 154 days
- Product code: NHA (Abutment, Implant, Dental, Endosseous)
- Device class: 2
- Regulation: 21 CFR 872.3630
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
15 later devices descend from it; 2 cite it directly.
0 of 16 devices 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) BIOMET 3i - PSR Overdenture Bar: named in the summary without a submission number
- (no number) BIOMET 3i - CAM StructSURE Overdenture Bars: named in the summary without a submission number

## Most influential descendants
- K122424: Isus Implant Suprastructures (2013), 13 descendants of its own
- K160207: ATLANTIS ISUS Implant Suprastructures (2016), 5 descendants of its own
- K212676: Osteon Precision Milled Suprastructure (2022), 4 descendants of its own
- K163350: Multibase Abutments EV and ATLANTIS Suprastructures (2017), 4 descendants of its own
- K221019: Osteon Precision Milled Suprastructure (2022), 3 descendants of its own

## Indications for use
The 3i Patient-Specific CAM StructSURE Overdenture Bars are intended for use as an accessory to endosseous dental implants to support a prosthetic device in a partially or edentulous patient.

Source page: https://510kreport.com/device/K101582
Methodology: https://510kreport.com/methodology