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

ATEC Alignment App

K Number: K211987 · Decision Oct 29, 2021
Classifications
1
FEI Numbers
609
Registration Numbers
609
Same Product Code
2221
Applicant Total
46
Review Days
123

Basic Information

Device Name
ATEC Alignment App
K Number
K211987
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.2050
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Alphatec Spine, Inc.
Date Received
June 28, 2021
Decision Date
October 29, 2021
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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