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

Patient Specific Planning Solution™ 3D Bone Models

K Number: K230540 · Decision Jul 25, 2023
Classifications
1
FEI Numbers
599
Registration Numbers
599
Same Product Code
2271
Applicant Total
93
Review Days
148

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Basic Information

Device Name
Patient Specific Planning Solution™ 3D Bone Models
K Number
K230540
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.2050
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Biomet Manufacturing Corp
Date Received
February 27, 2023
Decision Date
July 25, 2023
Product Code
LLZ
Advisory Committee
Radiology
Review Advisory Committee
RA
Third Party
N

Classifications

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

Product Code Device Name
LLZ System, Image Processing, Radiological

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