STRAUMANN GUIDED INSTRUMENTS— 510(k) K082532

Substantially Equivalent

Straumann USA

FDA 510(k) clearance K082532 for STRAUMANN GUIDED INSTRUMENTS, Substantially Equivalent on 2008-10-21. Applicant: Straumann USA.

Clearance details

Applicant
Straumann USA
Product code
Code DZI
Advisory panel
Dental
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Andover, MA, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.