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510(k) Data Aggregation
K Number
K003045Device Name
HA-TI (HAND TITANIUM SCREW) IMPLANT
Manufacturer
HATI DENTAL AG.
Date Cleared
2001-07-12
(286 days)
Product Code
DZE
Regulation Number
872.3640Why did this record match?
Applicant Name (Manufacturer) :
HATI DENTAL AG.
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
Intended Use
Device Description
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