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

Anteralign LS coverplate

K Number: K260810 · Decision Jun 10, 2026
Classifications
1
FEI Numbers
253
Registration Numbers
253
Same Product Code
200
Applicant Total
31
Review Days
90

Basic Information

Device Name
Anteralign LS coverplate
K Number
K260810
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3080
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Tyber Medical, LLC
Date Received
March 12, 2026
Decision Date
June 10, 2026
Product Code
OVD
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
OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar

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