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

IMPLANT CENTER

K Number: K072030 · Decision Nov 19, 2007
Classifications
1
FEI Numbers
78
Registration Numbers
78
Same Product Code
48
Applicant Total
11
Review Days
118

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Basic Information

Device Name
IMPLANT CENTER
K Number
K072030
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.4120
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Satelec - Acteon Group
Date Received
July 24, 2007
Decision Date
November 19, 2007
Product Code
DZI
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
DZI Drill, Bone, Powered

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Other Clearances by Satelec - Acteon Group

K Number Device Name
K233922 SP NEWTRON CAN-A; MODULE NEWTRON CAN-A EMB; SUPPORT XINETIC; NWT CAN SLIM LED CORD G3 SHORT; NWT CAN SLIM LED CORD G3 LONG
K172137 PIEZOTOME CUBE
K131906 SCANWAVE PEN (WITH LIGHT GRAY CORD), SCANWAVE PEN (WITH MEDIUM GRAY CORD), SCANWAVE PEN (WITH DARK GRAY CORD), SCANWAVE
K132322 NEWTRON P5 XS B.LED
K132267 NEWTRON P5, NEWTRON P5 B.LED
K131151 ENDOCENTER
K131997 NEWTRON BOOSTER
K113430 PROULTRA PIEZO ULTRASONIC
K111623 I-ENDO DUAL
K071424 PMAX NEWTRON XS
Search all 11 clearances from Satelec - Acteon Group →