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

MCS Bone Graft

K Number: K162860 · Decision Feb 13, 2017
Classifications
1
FEI Numbers
229
Registration Numbers
229
Same Product Code
491
Applicant Total
5
Review Days
124

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Basic Information

Device Name
MCS Bone Graft
K Number
K162860
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3045
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Bioventus, LLC
Date Received
October 12, 2016
Decision Date
February 13, 2017
Product Code
MQV
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
MQV Filler, Bone Void, Calcium Compound

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K Number Device Name
K243782 StimTrial Neuromodulation System
K243678 TalisMann Neuromodulation System
K233368 Allograft Delivery Device (OFAC-C)
K233490 SIGNAFUSE Bioactive Strip (SBS); SIGNAFUSE Putty