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

MODUS SAGITTAL SPLIT PLATE

K Number: K993862 · Decision Dec 29, 1999
Classifications
1
FEI Numbers
106
Registration Numbers
106
Same Product Code
291
Applicant Total
14
Review Days
44

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Basic Information

Device Name
MODUS SAGITTAL SPLIT PLATE
K Number
K993862
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.4760
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
The Straumann Co.
Date Received
November 15, 1999
Decision Date
December 29, 1999
Product Code
JEY
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
JEY Plate, Bone

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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
K962023 PLASTIC PROTECTION HEALING CAPS
K960634 TITANIUM HEALING CAPS
K955281 ENDOSSEOUS DENTAL IMPLANT & ACCESSORIES
K955369 MEMFIX
K941393 ITI ANGLED ABUTMENT
K943720 ITI TRANSVERSAL SCREWING SYSTEM
K931993 ITI DISTANCE SYSTEM
Search all 14 clearances from The Straumann Co. →