FDA 510(k) FDA class 1 Substantially Equivalent 🇨🇦 Canada

ARTHROBOT(TM) WRIST HOLDER ACCESSORY

K Number: K911522 · Decision Apr 29, 1991
Classifications
1
FEI Numbers
24
Registration Numbers
24
Same Product Code
9
Applicant Total
16
Review Days
25

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
ARTHROBOT(TM) WRIST HOLDER ACCESSORY
K Number
K911522
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4960
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Andronic Devices, Ltd.
Date Received
April 4, 1991
Decision Date
April 29, 1991
Product Code
JEA
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
JEA Table, Surgical With Orthopedic Accessories, Ac-Powered

Similar 510(k) Clearances

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

View all

Other Clearances by Andronic Devices, Ltd.

K Number Device Name
K940812 INSIGHT ELECTRONIC ALIGNMENT INDICATOR
K934926 INSITE MODEL 20 & MODEL 15 INSUFFLATORS
K934928 INSITE FILTER & TUBING SET
K935381 KAPS POSITIONING ARM
K934124 AUTOQUOT AUTOMATED ALIQUOTTING SYSTEM
K936308 ENDEX ENDOSCOPIC POSITIONING SYSTEM
K932253 ARTHROBOT BI-FOLD DRAPE
K922625 ADEPT ENDOSCOPIC POSITIONER
K922626 ADEPT INSTRUMENT POSITIONING ACCESSORY
K911520 ARTHROBOT(TM) 75 (190 CM) GENERAL PURPOSE DRAPE
Search all 16 clearances from Andronic Devices, Ltd. →