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

RADIOGRAPHIC MARKERS

K Number: K011856 · Decision Aug 22, 2001
Classifications
1
FEI Numbers
102
Registration Numbers
102
Same Product Code
109
Applicant Total
85
Review Days
70

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Basic Information

Device Name
RADIOGRAPHIC MARKERS
K Number
K011856
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4300
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Encore Orthopedics, Inc.
Date Received
June 13, 2001
Decision Date
August 22, 2001
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

Similar 510(k) Clearances

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Other Clearances by Encore Orthopedics, Inc.

K Number Device Name
K032905 3DKNEE POROUS COATED FEMORAL COMPONENT
K020114 3D KNEE
K020741 UNICONDYLAR KNEE
K020236 MODIFICATION TO PASS SPINAL SYSTEM
K020170 KEYSTONE HIP SYSTEM CALCAR REPLACEMENT BODY AND BUILD UP
K013490 CEMENTED CALCAR HIP SYSTEM
K013442 PASS SPINAL SYSTEM
K003324 PLASMA SPRAYED SHOULDER
K013431 PASS SPINAL SYSTEM
K013191 PASS SPINAL SYSTEM
Search all 85 clearances from Encore Orthopedics, Inc. →