PERFORATED BIOABSORBABLE INTERFERENCE SCREW MEGAFIX

Screw, Fixation, Bone

KARL STORZ ENDOSCOPY

The following data is part of a premarket notification filed by Karl Storz Endoscopy with the FDA for Perforated Bioabsorbable Interference Screw Megafix.

Pre-market Notification Details

Device IDK030848
510k NumberK030848
Device Name:PERFORATED BIOABSORBABLE INTERFERENCE SCREW MEGAFIX
ClassificationScrew, Fixation, Bone
Applicant KARL STORZ ENDOSCOPY 600 CORPORATE POINTE Culver City,  CA  90230 -7600
ContactPaul S Lee
CorrespondentPaul S Lee
KARL STORZ ENDOSCOPY 600 CORPORATE POINTE Culver City,  CA  90230 -7600
Product CodeHWC  
CFR Regulation Number888.3040 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received2003-03-17
Decision Date2003-06-02
Summary:summary

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