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

ACE MOS SAW AND THE ACE MOS SPINE SAW

K Number: K862504 · Decision Aug 7, 1986
Classifications
1
FEI Numbers
36
Registration Numbers
37
Same Product Code
22
Applicant Total
111
Review Days
37

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Basic Information

Device Name
ACE MOS SAW AND THE ACE MOS SPINE SAW
K Number
K862504
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.4580
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Applicant
Buckman Co., Inc.
Date Received
July 1, 1986
Decision Date
August 7, 1986
Product Code
JDX
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
JDX Instrument, Surgical, Sonic And Accessory/Attachment

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K945756 IMAGN(TM) 2000 SYSTEM
K940003 VOLUMET CD4 + AND CD8 + T LYMPHOCYTE COUNT TEST KIT
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