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

KARL STORZ MEGAFIX-T TITANIUM INTERFERENCE SCREW

K Number: K030368 · Decision Mar 20, 2003
Classifications
1
FEI Numbers
659
Registration Numbers
659
Same Product Code
1058
Applicant Total
334
Review Days
44

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
KARL STORZ MEGAFIX-T TITANIUM INTERFERENCE SCREW
K Number
K030368
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-America, Inc.
Date Received
February 4, 2003
Decision Date
March 20, 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

Similar 510(k) Clearances

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

View all

Other Clearances by KARL STORZ Endoscopy-America, Inc.

K Number Device Name
K252624 KARL STORZ Laryngoscopes and Accessories
K223923 HOPKINS Telescopes
K202957 Flexible Video Cysto-Urethroscope (C-view)
K200318 UNIDRIVE S II ENT, DrillCut-X II-35 Shaver Handpiece, DrillCut-X II-35 N Shaver Handpiece
K201135 Image1 S CCU, Image1 S 4U Camera Head
K200740 HD Video Rhino Laryngoscope
K191357 Flexible HD Cysto-Urethroscope System
K182723 Flexible HD Cysto-Urethroscope System
K182186 CMOS Video-Rhino-Laryngoscope System
K183264 Flex-THOR scope
Search all 334 clearances from KARL STORZ Endoscopy-America, Inc. →