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

Uni-FuZe-P Bone Putty

K Number: K201781 · Decision Dec 28, 2020
Classifications
1
FEI Numbers
229
Registration Numbers
229
Same Product Code
491
Applicant Total
30
Review Days
181

Basic Information

Device Name
Uni-FuZe-P Bone Putty
K Number
K201781
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3045
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Zavation Medical Products, LLC
Date Received
June 30, 2020
Decision Date
December 28, 2020
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

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (MQV), ordered by most recent decision date.

View all

Other Clearances by Zavation Medical Products, LLC

K Number Device Name
K243908 Tiger 2 System
K233509 Zavation IBF System, Zavation Varisync Plate System and Varisync Spacer System, LABYRINTH System, Zavation ALIF System
K231811 Zavation Connector System
K223808 Zavation Navigation Instrument System
K230731 Zavation ALIF System
K221726 Uni-FuZe-C Bone Strip
K222614 Zavation Spinal System
K221049 Zavation VariSync Plate System and VariSync Spacer System
K220581 Zavation eZspand Interbody System
K212811 Ti3Z Lumbar Interbody System
Search all 30 clearances from Zavation Medical Products, LLC →