FDA 510(k) FDA class 2 Substantially Equivalent 🇯🇵 Japan

OSTEOTRANS -MX BIOABSORBABLE BONE FIXATION SYSTEM

K Number: K061881 · Decision Mar 14, 2007
Classifications
1
FEI Numbers
106
Registration Numbers
106
Same Product Code
291
Applicant Total
6
Review Days
254

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Basic Information

Device Name
OSTEOTRANS -MX BIOABSORBABLE BONE FIXATION SYSTEM
K Number
K061881
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.4760
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Takiron Co., Ltd.
Date Received
July 3, 2006
Decision Date
March 14, 2007
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

Similar 510(k) Clearances

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

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Other Clearances by Takiron Co., Ltd.

K Number Device Name
K081390 BIOACTIF OSTEOTRANS INTERFENCE SCREW
K073006 OSTEOTRANS -MX BIOABSORBABLE BONE FIXATION SYSTEM
K073312 OSTEOTRANS-OT SCREW
K073311 OSTEOTRANS-OT PIN
K062691 COMPORUS