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IntraOp Alignment System

Page Type
Cleared 510(K)
510(k) Number
K240199
510(k) Type
Traditional
Applicant
Alphatec Spine, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/22/2024
Days to Decision
118 days
Submission Type
Summary

IntraOp Alignment System

Page Type
Cleared 510(K)
510(k) Number
K240199
510(k) Type
Traditional
Applicant
Alphatec Spine, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/22/2024
Days to Decision
118 days
Submission Type
Summary