FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

Endiscope, Endiscope Cervical

K Number: K180766 · Decision Jun 11, 2018
Classifications
1
FEI Numbers
386
Registration Numbers
386
Same Product Code
680
Applicant Total
8
Review Days
80

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
Endiscope, Endiscope Cervical
K Number
K180766
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.1100
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Elliquence, LLC
Date Received
March 23, 2018
Decision Date
June 11, 2018
Product Code
HRX
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
HRX Arthroscope

Similar 510(k) Clearances

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

View all

Other Clearances by Elliquence, LLC

K Number Device Name
K243739 AxCess® Expandable Interbody System
K170107 Surgi Max Ultra
K162490 Disc-FX System
K160041 Cobbra RF Tissue Dissector
K142410 Elliquence Electrodes
K130110 MEDDUSA BIPOLAR SYSTEM
K100390 SURGIMAX/ SURGIMAX PLUS