510(k) K860360

Device
KYOCERA BIOCERAM POROUS DENTAL IMPLANT
Applicant
KYOCERA INTERNATIONAL, INC.
510(k) number
K860360
Product code
DZE  
Decision
Substantially Equivalent (SESE)
Decision date
1986-04-04
Date received
1986-01-30
Regulation
872.3640
Classification name
Implant, Endosseous, Root-form
Medical specialty
Dental
Review panel
Dental
Device class
2
Clearance type
Traditional
Third party reviewed
No

Related Records

Applicant Contact

Contact
BARRY CALVARESE
Address
8611 Balboa Ave. San Diego CA US 92123 92123

FDA Registration Numbers

Source Documents

510(k) summary PDF not indicated by FDA

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Legacy Summary

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FDA Review

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