FDA 510(k) FDA class 2 Substantially Equivalent 🇸🇪 Sweden

BRANEMARK INTEGRATION BIOHELIX IMPLANTS

K Number: K090005 · Decision May 19, 2009
Classifications
1
FEI Numbers
324
Registration Numbers
324
Same Product Code
1545
Applicant Total
3
Review Days
137

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Basic Information

Device Name
BRANEMARK INTEGRATION BIOHELIX IMPLANTS
K Number
K090005
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
872.3640
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Branemark Integration AB
Date Received
January 2, 2009
Decision Date
May 19, 2009
Product Code
DZE
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
DZE Implant, Endosseous, Root-Form

Similar 510(k) Clearances

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

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Other Clearances by Branemark Integration AB

K Number Device Name
K040643 BRANEMARK INTEGRATION DENTAL IMPLANT AND ACCESSORIES
K021355 ENDOSSEOUS IMPLANT