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

CANNULATED LAG SCREWS

K Number: K863119 · Decision Sep 3, 1986
Classifications
1
FEI Numbers
283
Registration Numbers
283
Same Product Code
203
Applicant Total
60
Review Days
20

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Basic Information

Device Name
CANNULATED LAG SCREWS
K Number
K863119
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3040
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Applicant
Downs Surgical , Ltd.
Date Received
August 14, 1986
Decision Date
September 3, 1986
Product Code
HTY
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
HTY Pin, Fixation, Smooth

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