FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

ENDOTOME PNEUMATIC ORTHOPAEDIC CUT

K Number: K840831 · Decision Apr 4, 1984
Classifications
1
FEI Numbers
67
Registration Numbers
67
Same Product Code
55
Applicant Total
38
Review Days
40

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Basic Information

Device Name
ENDOTOME PNEUMATIC ORTHOPAEDIC CUT
K Number
K840831
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4820
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Cabot Medical Corp.
Date Received
February 24, 1984
Decision Date
April 4, 1984
Product Code
HSZ
Advisory Committee
General, Plastic Surgery
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
HSZ Instrument, Surgical, Orthopedic, Pneumatic Powered & Accessory/Attachment

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K951714 CABOT MEDICAL-SURGITEK ULTRAGOLD PLUS SIDE-FIRING UROLOGIC LASER FIBER
K941743 CABOT MEDICAL NIAGARA FLUID MANAGEMENT PUMP
K934115 3000 ELECTRONIC INSUFFLATOR MODIFICATION
K932293 CABOT MEDICAL BIPOLAR CUTTING FORCEPS
K930954 THE CABOT MEDICAL INSUL-SHETH VAGINAL SPECULUM COV
K932626 CABOT MEDICAL SURGIFLEX(R) SUCTION-IRRIGATION PROB
K935786 CORSON AND NEZHAT SUCTION/IRRIGATION PROBES
Search all 38 clearances from Cabot Medical Corp. →