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

SYNTHES MULTILOC PROXIMAL HUMERAL NAILING SYSTEM

K Number: K103002 · Decision Mar 2, 2011
Classifications
1
FEI Numbers
302
Registration Numbers
302
Same Product Code
528
Applicant Total
402
Review Days
145

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Basic Information

Device Name
SYNTHES MULTILOC PROXIMAL HUMERAL NAILING SYSTEM
K Number
K103002
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3020
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Synthes (Usa)
Date Received
October 8, 2010
Decision Date
March 2, 2011
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 Synthes (Usa)

K Number Device Name
K131984 SYNTHES SYNSONIC ULNA NAIL
K111667 SYNTHES SUPRAPATELLAR INSERTION INSTRUMENTS
K111540 SYNTHES 3.5MM LCP CLAVICLE PLATE SYSTEM
K110789 SYNTHES STERNAL ZIPFIX SYSTEM
K103243 2.4MM VA-LCP INTERCARPAL FUSION SYSTEM
K102656 SYNTHES DENTOALVEOLAR BONE FIXATION SYSTEM
K093299 SYNTHES ORTHODONTIC BONE ANCHOR SYSTEM
K102694 2.4MM VA-LCP DORSAL DISTAL RADIUS PLATES
K100776 SYNTHES 2.4 MM/2.7 MM VARIABLE ANGLE LCP FOREFOOT/MIDFOOT SYSTEM
K100634 SYNTHES MATRIX SYSTEM
Search all 402 clearances from Synthes (Usa) →