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

ACUMED ANATOMIC RADIAL HEAD SYSTEM

K Number: K041858 · Decision Oct 5, 2004
Classifications
1
FEI Numbers
101
Registration Numbers
101
Same Product Code
32
Applicant Total
38
Review Days
88

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Basic Information

Device Name
ACUMED ANATOMIC RADIAL HEAD SYSTEM
K Number
K041858
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3170
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Acumed, LLC
Date Received
July 9, 2004
Decision Date
October 5, 2004
Product Code
KWI
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
KWI Prosthesis, Elbow, Hemi-, Radial, Polymer

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K243624 Acu-Sinch Knotless Mini
K233311 Acumed Wrist Plating System
K230744 Acumed Acutrak 3 Headless Compression Screw System
K221333 Acumed Acutrak System- MR Conditional, Acumed Acturak 2 System- MR Conditional
K212990 Acumed Ankle Syndesmosis Repair System
K210750 Acumed Clavicle Hook Plating System
K151886 Acumed Ankle and Small Fragment Base Set Update
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