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

THE STRAUMANN ORTHO IMPLANT SYSTEM

K Number: K040469 · Decision Apr 30, 2004
Classifications
1
FEI Numbers
54
Registration Numbers
54
Same Product Code
51
Applicant Total
14
Review Days
66

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Basic Information

Device Name
THE STRAUMANN ORTHO IMPLANT SYSTEM
K Number
K040469
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3640
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
The Straumann Co.
Date Received
February 24, 2004
Decision Date
April 30, 2004
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 The Straumann Co.

K Number Device Name
K041070 STRAUMANN TEMPORARY COPING
K040646 STRAUMANN GRANULES
K993862 MODUS SAGITTAL SPLIT PLATE
K962023 PLASTIC PROTECTION HEALING CAPS
K960634 TITANIUM HEALING CAPS
K955281 ENDOSSEOUS DENTAL IMPLANT & ACCESSORIES
K955369 MEMFIX
K941393 ITI ANGLED ABUTMENT
K943720 ITI TRANSVERSAL SCREWING SYSTEM
K931993 ITI DISTANCE SYSTEM
Search all 14 clearances from The Straumann Co. →