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

Talon DistalFix Antegrade/Retrograde Femoral Nail

K Number: K152295 · Decision Nov 3, 2015
Classifications
1
FEI Numbers
302
Registration Numbers
302
Same Product Code
528
Applicant Total
4
Review Days
82

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Basic Information

Device Name
Talon DistalFix Antegrade/Retrograde Femoral Nail
K Number
K152295
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3020
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Orthopedic Designs North America, Inc.
Date Received
August 13, 2015
Decision Date
November 3, 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

Similar 510(k) Clearances

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

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Other Clearances by Orthopedic Designs North America, Inc.

K Number Device Name
K210146 Cannulated Compression Device System
K173255 Talon DistalFix Humeral Nail
K111352 TALON DISTALFIX PROXIMAL FEMORAL NAIL