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

KSEA SPINOSCOPE

K Number: K023187 · Decision Dec 2, 2002
Classifications
1
FEI Numbers
368
Registration Numbers
368
Same Product Code
669
Applicant Total
35
Review Days
69

Basic Information

Device Name
KSEA SPINOSCOPE
K Number
K023187
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.1100
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
KARL STORZ ENDOSCOPY
Date Received
September 24, 2002
Decision Date
December 2, 2002
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 KARL STORZ ENDOSCOPY

K Number Device Name
K043375 FISCH TITANIUM MIDDLE EAR PROSTHESES
K030848 PERFORATED BIOABSORBABLE INTERFERENCE SCREW MEGAFIX
K030009 KSEA POWERSHAVER SYSTEM S2
K023924 AUTOCON II 200 ELECTROSURGICAL GENERATOR
K011700 MODULITH SLK LITHOTRIPTER
K021776 KSEA QUADRO SWITCH
K013107 BIOABSORBABLE INTERFERENCE SCREW MEGAFIX
K011841 KSEA SAWAHLE ELECTROMECHANICAL MORCELLATOR
K010569 KSEA UNIVERSAL LAPAROMAT LAPAROSCOPIC SUCTION AND IRRIGATION PUMP
K004037 X-RAY SYSTEM XR-MX
Search all 35 clearances from KARL STORZ ENDOSCOPY →