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Precice Intramedullary Limb Lengthening System

Page Type
Cleared 510(K)
510(k) Number
K220234
510(k) Type
Traditional
Applicant
Nuvasive Specialized Orthopedics, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/15/2023
Days to Decision
412 days
Submission Type
Summary

Precice Intramedullary Limb Lengthening System

Page Type
Cleared 510(K)
510(k) Number
K220234
510(k) Type
Traditional
Applicant
Nuvasive Specialized Orthopedics, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/15/2023
Days to Decision
412 days
Submission Type
Summary