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

CRANION CRANIAL FIXATION SYSTEM; FIXLOCK; CRANIAL SOLUTIONS; CEREMED FIXATION SYSTEM

K Number: K051293 · Decision Jun 14, 2005
Classifications
1
FEI Numbers
106
Registration Numbers
106
Same Product Code
291
Applicant Total
20
Review Days
27

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Basic Information

Device Name
CRANION CRANIAL FIXATION SYSTEM; FIXLOCK; CRANIAL SOLUTIONS; CEREMED FIXATION SYSTEM
K Number
K051293
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.4760
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Ceremed , Inc.
Date Received
May 18, 2005
Decision Date
June 14, 2005
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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K132198 ADAPTAIN, ADAPTAIN FASTWRAP, ENVELOCK, BIOWAI
K122561 ADAPTAIN FASTWRAP, ENVELOCK, GRAFTAIN
K120220 ADAPTAIN SOLUBLE IMPLANT MATERIAL
K103047 CERETENE SOLUBLE IMPLANT MATERIAL
K102071 OSTENE CT, AOC CT, OSTEOTENE, CERETENE
K091636 OSTENE CT, AOC CT, OSTEOTENE, CERETENE
K082491 OSTENE CT SOLUBLE BONE HEMOSTASIS IMPLANT MATERIAL, AOC CT, AOC, OSTENE, OSTEOTENE & CERETENE
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