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

STRAUMANN TEMPORARY COPING

K Number: K041070 · Decision Jul 23, 2004
Classifications
1
FEI Numbers
382
Registration Numbers
382
Same Product Code
708
Applicant Total
14
Review Days
88

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Basic Information

Device Name
STRAUMANN TEMPORARY COPING
K Number
K041070
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3630
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
The Straumann Co.
Date Received
April 26, 2004
Decision Date
July 23, 2004
Product Code
NHA
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
NHA Abutment, Implant, Dental, Endosseous

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Other Clearances by The Straumann Co.

K Number Device Name
K040646 STRAUMANN GRANULES
K040469 THE STRAUMANN ORTHO IMPLANT SYSTEM
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. →