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

ARTHROSCOPIC SHOULDER HOLDER

K Number: K870212 · Decision Feb 20, 1987
Classifications
1
FEI Numbers
205
Registration Numbers
205
Same Product Code
37
Applicant Total
19
Review Days
31

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Basic Information

Device Name
ARTHROSCOPIC SHOULDER HOLDER
K Number
K870212
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
888.5850
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Applicant
Dyonics, Inc.
Date Received
January 20, 1987
Decision Date
February 20, 1987
Product Code
HST
Advisory Committee
Orthopedic
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
HST Apparatus, Traction, Non-Powered

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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. →