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

HARRINGTON-TYPE INSTRU-SCOLIOSIS

K Number: K840423 · Decision Mar 23, 1984
Classifications
1
FEI Numbers
321
Registration Numbers
321
Same Product Code
429
Applicant Total
21
Review Days
52

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Basic Information

Device Name
HARRINGTON-TYPE INSTRU-SCOLIOSIS
K Number
K840423
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3050
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Applicant
Link America, Inc.
Date Received
January 31, 1984
Decision Date
March 23, 1984
Product Code
KWP
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
KWP Appliance, Fixation, Spinal Interlaminal

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