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

MONDEAL CONTOUR HO SYSTEM

K Number: K050657 · Decision Aug 8, 2005
Classifications
1
FEI Numbers
519
Registration Numbers
519
Same Product Code
1313
Applicant Total
9
Review Days
147

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Basic Information

Device Name
MONDEAL CONTOUR HO SYSTEM
K Number
K050657
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3030
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Kapp Surgical Instrument, Inc.
Date Received
March 14, 2005
Decision Date
August 8, 2005
Product Code
HRS
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
HRS Plate, Fixation, Bone

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K050655 MONDEAL RADIUS HO SYSTEM, MODEL KS-MR-2005
K033930 KAPP CUSTOM ULNAR HEAD WRIST IMPLANT
K030237 KAPP CUSTOM RADIAL HEAD ELBOW IMPLANT
K844177 COSGROVE MITRAL VALVE RETRACTOR
K843368 KAPP SPINAL BUTTON