Inion Spinal Graft Containment System— 510(k) K151360

Unknown

Inion OY

FDA 510(k) clearance K151360 for Inion Spinal Graft Containment System, Unknown on 2015-10-06. Applicant: Inion OY. Device class: 2.

Clearance details

Applicant
Inion OY
Product code
Code OJB
Device class
Class 2
Regulation
21 CFR 888.3060
Advisory panel
Orthopedic
Date received
Decision date
Decision
Unknown
Clearance type
Traditional
Location
Tampere, FI
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