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

HUCKSTEP INTRAMEDULLARY NAIL

K Number: K811017 · Decision May 27, 1981
Classifications
1
FEI Numbers
249
Registration Numbers
249
Same Product Code
403
Applicant Total
60
Review Days
42

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Basic Information

Device Name
HUCKSTEP INTRAMEDULLARY NAIL
K Number
K811017
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3030
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Applicant
Downs Surgical , Ltd.
Date Received
April 15, 1981
Decision Date
May 27, 1981
Product Code
KTT
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
KTT Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component

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K Number Device Name
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K903748 ISLAM STERNAL PUNCTURE NEEDLE, CAT # AF-594-00-V
K903750 ISLAM STERNAL PUNCTURE NEEDLE, CAT #AG-598-OO-E
K903747 ISLAM STERNAL PUNCTURE NEEDLE, CAT # AG-592-00-U
K900611 SHEPPERD DILATATION TUBE SET (GS-501-20-H)
K900614 SHEPPERD SHORT MUSCLE RETRACTOR (GS-501-45-V)
K900612 SHEPPERD TREPHINE SET (GS-501-30-V)
K900610 SHEPPERD CANNULA STILLETTE & OBDURATOR SET
K900616 SHEPPERD CUTTING FORCEPS
K900609 SHEPPERD STRAIGHT AND CURVED NEEDLES
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