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

MODIFIED SAW BLADES TO THE SAGITAL SAW

K Number: K884839 · Decision Dec 7, 1988
Classifications
1
FEI Numbers
81
Registration Numbers
81
Same Product Code
28
Applicant Total
19
Review Days
16

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Basic Information

Device Name
MODIFIED SAW BLADES TO THE SAGITAL SAW
K Number
K884839
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4820
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Dyonics, Inc.
Date Received
November 21, 1988
Decision Date
December 7, 1988
Product Code
KIJ
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
KIJ Instrument, Surgical, Orthopedic, Dc-Powered Motor And Accessory/Attachment

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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
K881876 DYNAMIC CRUCIATE TESTER
K880739 DYONICS DRILL GUIDE/ISOMETER SYSTEM
K880150 PACESETTER (TM) 3500 ARTHROSCOPIC SURGICAL SYSTEM
K870212 ARTHROSCOPIC SHOULDER HOLDER
Search all 19 clearances from Dyonics, Inc. →