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

GUIDE TO THE KNEE

K Number: K843121 · Decision Sep 7, 1984
Classifications
1
FEI Numbers
151
Registration Numbers
151
Same Product Code
19
Applicant Total
19
Review Days
30

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Basic Information

Device Name
GUIDE TO THE KNEE
K Number
K843121
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4950
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Dyonics, Inc.
Date Received
August 8, 1984
Decision Date
September 7, 1984
Product Code
BWN
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
BWN Table And Attachments, Operating-Room

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Other Clearances by Dyonics, Inc.

K Number Device Name
K900070 MODIFIED USES OF THE ARTHROSCOPIC SURGICAL SYSTEM
K896416 DYONICS SHOULDER PORTAL SYSTEM
K893136 SURGI-PAK FOR ARTHROSCOPIC ACROMIOPLASTY
K890665 MODIFIED CANNULA, TROCAR AND OBTURATOR ACCESSORIES
K894728 DYONICS DISPOSABLE ARTHROSCOPIC SURGICAL KNIFE
K892062 PS3500 ARTHROSCOPIC SURGICAL SYSTEM
K884839 MODIFIED SAW BLADES TO THE SAGITAL SAW
K881876 DYNAMIC CRUCIATE TESTER
K880739 DYONICS DRILL GUIDE/ISOMETER SYSTEM
K880150 PACESETTER (TM) 3500 ARTHROSCOPIC SURGICAL SYSTEM
Search all 19 clearances from Dyonics, Inc. →