FDA 510(k) FDA class 2 Substantially Equivalent 🇰🇷 South Korea

LOSPA IS TLIF & DLIF Cages

K Number: K170243 · Decision Mar 31, 2017
Classifications
1
FEI Numbers
418
Registration Numbers
418
Same Product Code
890
Applicant Total
33
Review Days
64

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Basic Information

Device Name
LOSPA IS TLIF & DLIF Cages
K Number
K170243
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
888.3080
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Corentec Co., Ltd.
Date Received
January 26, 2017
Decision Date
March 31, 2017
Product Code
MAX
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
MAX Intervertebral Fusion Device With Bone Graft, Lumbar

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K212034 LOSPA TKR System
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