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

BIOABSORBABLE INTERFERENCE SCREW MEGAFIX

K Number: K013107 · Decision Feb 26, 2002
Classifications
1
FEI Numbers
653
Registration Numbers
653
Same Product Code
1040
Applicant Total
35
Review Days
162

Basic Information

Device Name
BIOABSORBABLE INTERFERENCE SCREW MEGAFIX
K Number
K013107
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3040
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
KARL STORZ ENDOSCOPY
Date Received
September 17, 2001
Decision Date
February 26, 2002
Product Code
HWC
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
HWC Screw, Fixation, Bone

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K011841 KSEA SAWAHLE ELECTROMECHANICAL MORCELLATOR
K010569 KSEA UNIVERSAL LAPAROMAT LAPAROSCOPIC SUCTION AND IRRIGATION PUMP
K004037 X-RAY SYSTEM XR-MX
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