FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

MTI-MP TRANSITIONAL IMPLANTS AND MODULAR PROSTHETIC SYSTEM

K Number: K961704 · Decision Jul 26, 1996
Classifications
1
FEI Numbers
4
Registration Numbers
4
Same Product Code
5
Applicant Total
4
Review Days
85

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
MTI-MP TRANSITIONAL IMPLANTS AND MODULAR PROSTHETIC SYSTEM
K Number
K961704
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3890
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Dentatus USA , Ltd.
Date Received
May 2, 1996
Decision Date
July 26, 1996
Product Code
ELS
Advisory Committee
Dental
Review Advisory Committee
DE
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
ELS Splint, Endodontic Stabilizing

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (ELS), ordered by most recent decision date.

View all

Other Clearances by Dentatus USA , Ltd.

K Number Device Name
K042931 TUF LINK SILICONE RELINER
K031793 DENTATUS OSCIOMAT
K980620 DENTATUS MTI MODULAR TRANSITIONAL IMPLANTS AND PROSTHETIC SYSTEM