FDA.report

510(k) K193401

Device
Altatec GmbH CAMLOG/CONELOG PROGRESSIVE-LINE Implants
Applicant
Altatec GmbH
510(k) number
K193401
Product code
DZE
Decision
Substantially Equivalent (SESE)
Decision date
2020-09-29
Date received
2019-12-06
Regulation
872.3640
Classification name
Implant, Endosseous, Root-Form
Medical specialty
Dental
Review panel
Dental
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
No

Related Records

Applicant Contact

Contact
Reto Pusterla
Address
Maybachstrasse 5 Wimsheim DE D-71299 D-71299

FDA Registration Numbers

Source Documents

510(k) summary PDF

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