FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

SYNTHES ORTHODONTIC BONE ANCHOR SYSTEM

K Number: K093299 · Decision Dec 16, 2010
Classifications
1
FEI Numbers
54
Registration Numbers
54
Same Product Code
51
Applicant Total
402
Review Days
421

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Basic Information

Device Name
SYNTHES ORTHODONTIC BONE ANCHOR SYSTEM
K Number
K093299
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3640
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Synthes (Usa)
Date Received
October 21, 2009
Decision Date
December 16, 2010
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

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Other Clearances by Synthes (Usa)

K Number Device Name
K131984 SYNTHES SYNSONIC ULNA NAIL
K111667 SYNTHES SUPRAPATELLAR INSERTION INSTRUMENTS
K111540 SYNTHES 3.5MM LCP CLAVICLE PLATE SYSTEM
K110789 SYNTHES STERNAL ZIPFIX SYSTEM
K103002 SYNTHES MULTILOC PROXIMAL HUMERAL NAILING SYSTEM
K103243 2.4MM VA-LCP INTERCARPAL FUSION SYSTEM
K102656 SYNTHES DENTOALVEOLAR BONE FIXATION SYSTEM
K102694 2.4MM VA-LCP DORSAL DISTAL RADIUS PLATES
K100776 SYNTHES 2.4 MM/2.7 MM VARIABLE ANGLE LCP FOREFOOT/MIDFOOT SYSTEM
K100634 SYNTHES MATRIX SYSTEM
Search all 402 clearances from Synthes (Usa) →