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

PERFORATED BIOABSORBABLE INTERFERENCE SCREW MEGAFIX

K Number: K030848 · Decision Jun 2, 2003
Classifications
1
FEI Numbers
659
Registration Numbers
659
Same Product Code
1058
Applicant Total
35
Review Days
77

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Basic Information

Device Name
PERFORATED BIOABSORBABLE INTERFERENCE SCREW MEGAFIX
K Number
K030848
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
March 17, 2003
Decision Date
June 2, 2003
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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Other Clearances by Karl Storz Endoscopy

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K023187 KSEA SPINOSCOPE
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
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