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

MEMFIX

K Number: K955369 · Decision Jan 23, 1996
Classifications
1
FEI Numbers
71
Registration Numbers
71
Same Product Code
79
Applicant Total
14
Review Days
60

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Basic Information

Device Name
MEMFIX
K Number
K955369
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.4880
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
The Straumann Co.
Date Received
November 24, 1995
Decision Date
January 23, 1996
Product Code
DZL
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
DZL Screw, Fixation, Intraosseous

Similar 510(k) Clearances

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

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Other Clearances by The Straumann Co.

K Number Device Name
K041070 STRAUMANN TEMPORARY COPING
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
K941393 ITI ANGLED ABUTMENT
K943720 ITI TRANSVERSAL SCREWING SYSTEM
K931993 ITI DISTANCE SYSTEM
Search all 14 clearances from The Straumann Co. →