FDA 510(k) FDA class 2 Substantially Equivalent 🇩🇪 Germany

OsteoBridge™ IDSF System

K Number: K181026 · Decision Oct 17, 2018
Classifications
1
FEI Numbers
302
Registration Numbers
302
Same Product Code
528
Applicant Total
2
Review Days
182

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Basic Information

Device Name
OsteoBridge™ IDSF System
K Number
K181026
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
888.3020
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Merete GmbH
Date Received
April 18, 2018
Decision Date
October 17, 2018
Product Code
HSB
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
HSB Rod, Fixation, Intramedullary And Accessories

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K Number Device Name
K172213 MECRON Cannulated Screw System