FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇭 Switzerland

BONEFIT R SCREW IMPLANTS

K Number: K894595 · Decision Feb 13, 1990
Classifications
1
FEI Numbers
333
Registration Numbers
333
Same Product Code
1516
Applicant Total
36
Review Days
204

Basic Information

Device Name
BONEFIT R SCREW IMPLANTS
K Number
K894595
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3640
Medical Specialty
Dental
Decision
Substantially Equivalent
Applicant
INSTITUT STRAUMANN AG
Date Received
July 24, 1989
Decision Date
February 13, 1990
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

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Other Clearances by INSTITUT STRAUMANN AG

K Number Device Name
K162848 Straumann CARES Golden Ti/TiN Abutments
K162311 Straumann PrefGel
K153758 Straumann Bone Level Tapered Implants
K120822 STRAUMANN CARES VARIOBASE ABUTMENT NNC, STRAUMANN CARES VARIOBASE ABUTMENT RN, STRAUMANN CARES VARIOBASE ABUTMENT WN, ST
K101465 STRAUMANN CARES BRIDGE; STRAUMANN CARES DOLDER BAR
K091701 STRAUMANN MODIFIED DENTAL ABUTMENT
K093113 ETKON ES1, MODEL 019.0001, ETKON VISUAL, STRAUMANN CADCAM ABUTMENT
K082111 STRAUMANN MEMBRAGEL
K081419 STRAUMANN DENTAL IMPLANT SYSTEM
K082545 STRAUMANN NN CARES TITANIUM AND CERAMIC ABUTMENTS
Search all 36 clearances from INSTITUT STRAUMANN AG →