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

OSTEOTRANS-OT PIN

K Number: K073311 · Decision May 13, 2008
Classifications
1
FEI Numbers
283
Registration Numbers
283
Same Product Code
203
Applicant Total
6
Review Days
172

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Basic Information

Device Name
OSTEOTRANS-OT PIN
K Number
K073311
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3040
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Takiron Co., Ltd.
Date Received
November 23, 2007
Decision Date
May 13, 2008
Product Code
HTY
Advisory Committee
Orthopedic
Review Advisory Committee
OR
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
HTY Pin, Fixation, Smooth

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (HTY), 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
K062691 COMPORUS
K061881 OSTEOTRANS -MX BIOABSORBABLE BONE FIXATION SYSTEM