FDA 510(k) FDA class 2 Substantially Equivalent 🇬🇧 United Kingdom

SHEPPERD SHELTER TUBE COMPLETE & DRILL

K Number: K900613 · Decision Oct 22, 1990
Classifications
1
FEI Numbers
386
Registration Numbers
386
Same Product Code
680
Applicant Total
60
Review Days
256

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Basic Information

Device Name
SHEPPERD SHELTER TUBE COMPLETE & DRILL
K Number
K900613
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.1100
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Applicant
Downs Surgical , Ltd.
Date Received
February 8, 1990
Decision Date
October 22, 1990
Product Code
HRX
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
HRX Arthroscope

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Other Clearances by Downs Surgical , Ltd.

K Number Device Name
K903749 ISLAM STERNAL PUNCTURE NEEDLE, CAT #AG-596-00-U
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
Search all 60 clearances from Downs Surgical , Ltd. →