FDA 510(k) FDA class 2 Substantially Equivalent 🇫🇷 France

Idys® LIF

K Number: K243670 · Decision Dec 31, 2024
Classifications
1
FEI Numbers
418
Registration Numbers
418
Same Product Code
890
Applicant Total
10
Review Days
34

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Basic Information

Device Name
Idys® LIF
K Number
K243670
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
888.3080
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Clariance
Date Received
November 27, 2024
Decision Date
December 31, 2024
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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K240715 Idys® C ZP 3DTi
K220182 Aggeris™-C
K200919 Idys ALIF 3DTi
K130853 IDYS(TM) C
K131178 IDYS LIF CAGES
K120469 ERISMA-LP