FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇦 Canada

HSC UNIT ROD

K Number: K871870 · Decision Jul 21, 1987
Classifications
1
FEI Numbers
321
Registration Numbers
321
Same Product Code
429
Applicant Total
6
Review Days
69

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Basic Information

Device Name
HSC UNIT ROD
K Number
K871870
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3050
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Applicant
Research Development Corp.
Date Received
May 13, 1987
Decision Date
July 21, 1987
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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K771019 LUNG-MECHANICS MONITOR
K770785 MONITOR, RESPIRATORY, TWO-GAS, RDC
K770061 VO RESPIRATORY PNEUMOTACHOGRAPH