Search Results
Found 1 results
510(k) Data Aggregation
(89 days)
TRATE Dental Implant System
TRATE Dental Implant System is indicated for use in surgical and restorative applications for placement in the bone of the upper or lower jaw to provide support for prosthetic devices, such as artificial teeth, in order to restore the patient's chewing function. TRATE Dental Implant System is indicated also for immediate loading when good primary stability is achieved and with appropriate occlusal loading.
The TRATE Dental Implant System is an endosseous dental implant and abutment system consisting of screw-type implants manufactured of Titanium Alloy (Ti6AIV4. acc. to EN ISO 5832-3/ASTM F136). The implants are blasted with HAP / TCP for surface roughening, acid-etched and anodized. The cover screws, abutment fixation screws and abutments are made of Titanium Alloy (Ti6A14V). Some subject devices are surfaced anodized. TRATE Dental Implants are two-piece implants: TRATE Dental Implant System implant type is a two-component ROOTFORM implant with combined thread and tapered connection is intended for surgical placement in the upper or lower jaw to support crowns, bridges or overdentures in edentulous and partially edentulous jaws of patients in order to restore the patients chewing for single or multiple unit restorations. TRATE Dental Implant System implants are indicated also for immediate loading when good primary stability is achieved and with appropriate occlusal loading.
Here's a breakdown of the acceptance criteria and study information for the TRATE Dental Implant System, based on the provided document:
1. Table of Acceptance Criteria and Reported Device Performance
For medical devices like dental implants, "acceptance criteria" usually refer to performance specifications that the device must meet, often demonstrated through specific tests. The document mainly outlines a series of non-clinical tests rather than a statistical performance metric against clinical criteria.
Acceptance Criteria (Test/Standard) | Reported Device Performance / Evaluation Method |
---|---|
Biocompatibility (ISO 10993) | Testing conducted to evaluate biocompatibility. (Implied: Meets ISO 10993 standards). |
Bacterial Endotoxin Levels (ANSI/AAMI ST72) | Batch testing conducted on samples of water used in manufacturing (bimonthly) and from sterilized product (quarterly) to demonstrate levels |
Ask a specific question about this device
Page 1 of 1