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

SYNOCTA PROSTHETICS

K Number: K990342 · Decision Jul 20, 1999
Classifications
1
FEI Numbers
333
Registration Numbers
333
Same Product Code
1516
Applicant Total
41
Review Days
166

Basic Information

Device Name
SYNOCTA PROSTHETICS
K Number
K990342
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3640
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
STRAUMANN USA
Date Received
February 4, 1999
Decision Date
July 20, 1999
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 STRAUMANN USA

K Number Device Name
K151328 PURE Ceramic Implants
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K130808 STRAUMANN HEALING ABUTMENTS, HEALING CAPS, CLOSURE SCREWS
K122855 TL 04.1MM RN,S, SLACTIVE TIZR 6, 8, 10, 12, 14, 16MM DENTAL IMPLANTS
K121131 BL, 04.1 MM RC, SLACTIVE 8MM, TIZR AND 10MM, 12, 14MM
K113606 NNC GOLD ABUTMENT FOR BRIDGES
K113410 NNC SOLID ABUTMENT NNC TEMPORARY COPING FOR COLID ABUTMENT NNC TEMPORARY CAP FOR COLID ABUTMENT
K113283 NNC CEMENTABLE ABUTMENT STRAIGHT,15 DEGREE ANGLE, TYPE A ,15 DEGREE ANGLE, TYPE B,NNC BASAL SCREW CEMENTABLE ABUTMENTS
K112280 STRAUMANN CARES SCREW-RETAINED BRIDGE TITANIUM, STRAUMANN CARES DOLDER BAR TITANIUM
K111357 STRAUMANN NARROW NECK CROSSFIT (NNC) 03.3MM DENTAL IMPLANT SYSTEM
Search all 41 clearances from STRAUMANN USA →