FDA 510(k) FDA class 2 Substantially Equivalent 🇮🇹 Italy

LEONE ORTHODONTIC MINI IMPLANT

K Number: K071490 · Decision Feb 22, 2008
Classifications
1
FEI Numbers
54
Registration Numbers
54
Same Product Code
51
Applicant Total
4
Review Days
268

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Basic Information

Device Name
LEONE ORTHODONTIC MINI IMPLANT
K Number
K071490
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3640
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Leone S.P.A.
Date Received
May 30, 2007
Decision Date
February 22, 2008
Product Code
OAT
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
OAT Implant, Endosseous, Orthodontic

Similar 510(k) Clearances

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

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Other Clearances by Leone S.P.A.

K Number Device Name
K242944 Leone Orthodontic Implant TAD (Temporary Anchorage Device)
K070483 LEONE MONOIMPLANT FOR O-RING OVERDENTURE
K050586 LEONE IMPLANT SYSTEM