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

SELF-DRILLING RADIOGRAPHIC MARKER

K Number: K014148 · Decision Jan 17, 2002
Classifications
1
FEI Numbers
102
Registration Numbers
102
Same Product Code
109
Applicant Total
56
Review Days
30

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Basic Information

Device Name
SELF-DRILLING RADIOGRAPHIC MARKER
K Number
K014148
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
878.4300
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Walter Lorenz Surgical, Inc.
Date Received
December 18, 2001
Decision Date
January 17, 2002
Product Code
NEU
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
NEU Marker, Radiographic, Implantable

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Other Clearances by Walter Lorenz Surgical, Inc.

K Number Device Name
K063386 LORENZ ORTHODONTIC ANCHORAGE SYSTEM
K063052 LORENZ TITANIUM FRACTURE / RECONSTRUCTION DEVICES AND PRE-BENT PLATES
K063506 LORENZ STERNAL CLOSURE SYSTEM
K062842 TWIST DRILL
K061384 LORENZ PECTUS SUPPORT BAR, TITANIUM; LORENZ PECTUS SUPPORT BAR STABILIZER, TITANIUM
K042516 OTOMIMIX
K030425 LORENZ RESORBABLE DISTRACTION SYSTEM OR EXPANDER
K040990 MODIFICATION TO SELF-DRILLING RADIOGRAPHIC MARKERS
K040983 LORENZ SELF-DRILLING IMF SCREW
K033740 LORENZ STERNAL CLOSURE SYSTEM
Search all 56 clearances from Walter Lorenz Surgical, Inc. →