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

ORIO-Ti Intervertebral Body Fusion Cage System

K Number: K211935 · Decision Sep 30, 2021
Classifications
1
FEI Numbers
339
Registration Numbers
339
Same Product Code
348
Applicant Total
12
Review Days
100

Basic Information

Device Name
ORIO-Ti Intervertebral Body Fusion Cage System
K Number
K211935
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3080
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Spinecraft, LLC
Date Received
June 22, 2021
Decision Date
September 30, 2021
Product Code
ODP
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
ODP Intervertebral Fusion Device With Bone Graft, Cervical

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