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

CANNULATED FEMORAL NAIL

K Number: K954856 · Decision Mar 8, 1996
Classifications
1
FEI Numbers
17
Registration Numbers
17
Same Product Code
5
Applicant Total
402
Review Days
137

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Basic Information

Device Name
CANNULATED FEMORAL NAIL
K Number
K954856
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3060
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Synthes (Usa)
Date Received
October 23, 1995
Decision Date
March 8, 1996
Product Code
JDN
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
JDN Implant, Fixation Device, Spinal

Similar 510(k) Clearances

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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
K103002 SYNTHES MULTILOC PROXIMAL HUMERAL NAILING 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
Search all 402 clearances from Synthes (Usa) →