FDA 510(k) FDA class 1 Substantially Equivalent 🇦🇹 Austria

DRILLTECH, ISM, IMPLANTUNIT, ZIMMER SURGICAL MOTOR SYSTEM

K Number: K060287 · Decision May 3, 2006
Classifications
1
FEI Numbers
69
Registration Numbers
69
Same Product Code
60
Applicant Total
18
Review Days
86

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
DRILLTECH, ISM, IMPLANTUNIT, ZIMMER SURGICAL MOTOR SYSTEM
K Number
K060287
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
872.4200
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
W&H Dentalwerk Buermoos GmbH
Date Received
February 6, 2006
Decision Date
May 3, 2006
Product Code
EBW
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
EBW Controller, Foot, Handpiece And Cord

Similar 510(k) Clearances

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

View all

Other Clearances by W&H Dentalwerk Buermoos GmbH

K Number Device Name
K253776 Implantmed Plus II & Piezomed Plus II Module
K243280 Piezomed Pro (Piezomed Pro module M-PM100 incl. handpiece M-PH350, Piezomed Pro instruments (various tips) and accessories)
K201703 PROXEO Twist Cordless Polishing System PL-40 H
K181858 Electric Handpiece Motor
K171553 W&H Assistina Twin
K143704 Advanced Air System
K133488 PIEZOMED
K100600 PROSTHODONTIC SCREWDRIVER , MODEL IA-400
K083811 W&H HANDPIECE ANESTO, MODEL: RA-5
K090931 CORDLESS ENDO HANDPIECES EB-300, ENTRAN AND EB-300 S, S5 ENDO MOTOR
Search all 18 clearances from W&H Dentalwerk Buermoos GmbH →