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

ASTRA TECH IMPLANT SYSTEM, NEW COMPONENT

K Number: K072624 · Decision Oct 1, 2007
Classifications
1
FEI Numbers
382
Registration Numbers
382
Same Product Code
708
Applicant Total
10
Review Days
14

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Basic Information

Device Name
ASTRA TECH IMPLANT SYSTEM, NEW COMPONENT
K Number
K072624
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
872.3630
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Astra Tech AB
Date Received
September 17, 2007
Decision Date
October 1, 2007
Product Code
NHA
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
NHA Abutment, Implant, Dental, Endosseous

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K101005 ASTRA TECH IMPLANT SYSTEM, NEW COMPONENT
K101732 ASTRA TECH IMPLANT SYSTEM
K091239 ASTRA TECH IMPLANT SYSTEM
K080156 OSSEOSPEED TM PROFILE SYSTEM
K080396 OSSEOSPEED NARROW