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

DYNAMIC CRUCIATE TESTER

K Number: K881876 · Decision Nov 17, 1988
Classifications
1
FEI Numbers
0
Registration Numbers
0
Same Product Code
4
Applicant Total
19
Review Days
197

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Basic Information

Device Name
DYNAMIC CRUCIATE TESTER
K Number
K881876
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
890.1615
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Applicant
Dyonics, Inc.
Date Received
May 4, 1988
Decision Date
November 17, 1988
Product Code
LYH
Advisory Committee
Physical Medicine
Review Advisory Committee
NE
Third Party
N

Classifications

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

Product Code Device Name
LYH Arthrometer

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