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

MENISCAL SUTURING SYSTEM

K Number: K833943 · Decision Feb 27, 1984
Classifications
1
FEI Numbers
1106
Registration Numbers
1106
Same Product Code
57
Applicant Total
19
Review Days
104

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
MENISCAL SUTURING SYSTEM
K Number
K833943
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
888.4540
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Applicant
Dyonics, Inc.
Date Received
November 15, 1983
Decision Date
February 27, 1984
Product Code
LXH
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
LXH Orthopedic Manual Surgical Instrument

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (LXH), ordered by most recent decision date.

View all

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. →