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

REVOIS IMPLANT SYSTEM

K Number: K063106 · Decision Jun 11, 2007
Classifications
1
FEI Numbers
382
Registration Numbers
382
Same Product Code
708
Applicant Total
10
Review Days
243

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
REVOIS IMPLANT SYSTEM
K Number
K063106
Device Class
FDA class 2
Clearance Type
Abbreviated
Regulation Number
872.3630
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Curasan AG
Date Received
October 11, 2006
Decision Date
June 11, 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

Similar 510(k) Clearances

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

View all

Other Clearances by Curasan AG

K Number Device Name
K181721 Ceracell Ortho Foam
K160566 Cerasorb Ortho Foam
K111105 CURASAN OSSEOLIVE DENTAL
K103709 CERACELL DENTAL
K102872 OSBONE DENTAL
K100841 BONEOPTIMIZER
K040216 CERASORB M ORTHO
K031651 MODIFICATION TO CERASORB ORTHO
K014156 CERASORB ORTHO