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

PDQ AND PDQ-TI ABUTMENT

K Number: K990367 · Decision Apr 21, 1999
Classifications
1
FEI Numbers
324
Registration Numbers
324
Same Product Code
1545
Applicant Total
36
Review Days
75

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Basic Information

Device Name
PDQ AND PDQ-TI ABUTMENT
K Number
K990367
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3640
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Vident
Date Received
February 5, 1999
Decision Date
April 21, 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 Vident

K Number Device Name
K063768 TITANIUM SCALLOPED ABUTMENT
K060441 VITA VM 7, MODEL NX77 XXXX, NX78XXXX, NX79 XXXX; VITA VM 8, MODEL VX60 XXXX, VX61 XXXX, VX62 XXXX; VITA VM 9, MODEL NX98
K052710 VITA VM7, MODEL NX77 XXXX, NX78XXXX, NX79 XXXX; VITA VM 8, MODEL VX60 XXXX, VX61 XXXX, VX62 XXXX; VITA VM 9,
K052130 VITA IN-CERAM 2000 AL CUBES FOR INLAB, MODELS AL20/AL40
K050362 VITA PM 7 (20 GRAM BOTTLES), VITA PM 7 (50 GRAM BOTTLES)
K022996 VITA IN-CERAM YZ CUBES FOR CEREC
K012473 VIDENT HEXTOP, SYNOCTA IN-CERAM BLANK/COPING MANUFACTURED BY VIDENT
K000597 VITA RESPONSE
K984198 WIDE BODY ABUTMENTS
K982664 VITA TITANIUM PORCELAIN
Search all 36 clearances from Vident →