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

NOVABNE PUTTY BIOACTIVE SYNTHETIC BONE GRAFT

K Number: K112773 · Decision Oct 14, 2011
Classifications
1
FEI Numbers
229
Registration Numbers
229
Same Product Code
491
Applicant Total
30
Review Days
21

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Basic Information

Device Name
NOVABNE PUTTY BIOACTIVE SYNTHETIC BONE GRAFT
K Number
K112773
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
888.3045
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Novabone Products, LLC
Date Received
September 23, 2011
Decision Date
October 14, 2011
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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Other Clearances by Novabone Products, LLC

K Number Device Name
K242299 NovaBone Putty - Synthetic Bioactive Bone Graft
K240404 NovaBone Putty - Bioactive Synthetic Bone Graft (NB6600, NB6610, NB6615)
K220498 NovoGen Wound Matrix
K163310 NovaBone IRM
K152071 NovaBone MacroFORM MIS Composite - 2.5cc, NovaBone MIS Cartridge Delivery System (cartridge handle only)
K142712 Dental Collagen Wound Dressing (Nova Tape and NovaPlug)
K141207 NOVABONE BIOACTIVE STRIP
K140946 NOVABONE MACROFORM BIOACTIVE PACKABLE, NOVABONE MACROFORM BIOACTIVE COMPOSITE
K112428 NOVABONE DENTAL MORSELS - BIOACTIVE SYNTHETIC BONE GRAFT
K110925 NOVABONE MACROPOR-SI+ - BIOACTIVE BONE GRAFT
Search all 30 clearances from Novabone Products, LLC →