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

Sonoma Fibula Repair System

K Number: K142945 · Decision Jan 22, 2015
Classifications
1
FEI Numbers
302
Registration Numbers
302
Same Product Code
528
Applicant Total
9
Review Days
104

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Basic Information

Device Name
Sonoma Fibula Repair System
K Number
K142945
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3020
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Sonoma Orthopedic Products, Inc.
Date Received
October 10, 2014
Decision Date
January 22, 2015
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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Other Clearances by Sonoma Orthopedic Products, Inc.

K Number Device Name
K161371 Sonoma Fifth Metatarsal Repair System
K111550 SONOMA FASTRAC CLAVICLE FRACTURE REPAIR DEVICE MODEL SONOMA FASTRAC XXYYY(X=DIA, YYY=LENGTH- IN MM)
K100112 SOMONA CWG CLAVICLE FRACTURE REPAIR DEVICE MODEL SONOMA CWG XYYY(X=DIA, YYY=LENGTH-IN MM)
K092110 WAVEON FRACTURE REPAIR SYSTEM (WAVEON RX)
K090304 WAVEON WRX BONE FIXATION SYSTEM
K081832 ENSPLINTCMX CLAVICLE PIN
K080778 ENSPLINT TM BONE SCREW
K071809 ENSPLINTRX BONE FIXATION SYSTEM