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

STERNUM SAW

K Number: K801737 · Decision Aug 20, 1980
Classifications
1
FEI Numbers
15
Registration Numbers
15
Same Product Code
3
Applicant Total
19
Review Days
26

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Basic Information

Device Name
STERNUM SAW
K Number
K801737
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4820
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Amsco Co.
Date Received
July 25, 1980
Decision Date
August 20, 1980
Product Code
KFK
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
KFK Saw, Pneumatically Powered

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K832188 HALL RECIPROCATOR
K832187 HALL OSCILLATOR
K831086 CEILING MOUNTED SUPPORT
K832186 HALL DRILL/REAMER
K831309 DELIVERY 4 TABLE
K823360 SURGICAL LIGHT
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