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

Tritanium® TL Curved Posterior Lumbar Cage

K Number: K173476 · Decision Jan 18, 2018
Classifications
1
FEI Numbers
418
Registration Numbers
418
Same Product Code
890
Applicant Total
92
Review Days
70

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Basic Information

Device Name
Tritanium® TL Curved Posterior Lumbar Cage
K Number
K173476
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3080
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Stryker
Date Received
November 9, 2017
Decision Date
January 18, 2018
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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