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

ORTHOFIX ANKLE HINDFOOT NAILING SYSTEM

K Number: K141571 · Decision Nov 12, 2014
Classifications
1
FEI Numbers
295
Registration Numbers
295
Same Product Code
505
Applicant Total
15
Review Days
153

Basic Information

Device Name
ORTHOFIX ANKLE HINDFOOT NAILING SYSTEM
K Number
K141571
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3020
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
ORTHOFIX SRL
Date Received
June 12, 2014
Decision Date
November 12, 2014
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

Similar 510(k) Clearances

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

View all

Other Clearances by ORTHOFIX SRL

K Number Device Name
K161466 ORTHOFIX CHIMAERA Hip Fracture System - Trochanteric Nailing System
K153233 Galaxy UNYCO System
K152171 Orthofix TL-HEX True Lok Hexapod System (TL-HEX) V1.4
K141760 ORTHOFIX GALAXY WRIST
K142052 ORTHOFIX GALAXY UNYCO DIAPHYSEAL TIBIA KIT
K141078 ORTHOFIX TL-HEX TRUE LOK HEXALOBE SYSTEM (TL-HEX)
K122541 ORTHOFIX CONTOURS PROIMAL HUMERAL PLATE (PHP)
K113770 ORTHOFIX GALAXY FIXATION SYSTEM
K062920 ORTHOFIX TITANIUM HUMERAL PLATING SYSTEM LSP
K053261 ORTHOFIX TITANIUM NAILING SYSTEMS
Search all 15 clearances from ORTHOFIX SRL →