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PRECICE Intramedullary Limb Lengthening System

Page Type
Cleared 510(K)
510(k) Number
K170346
510(k) Type
Traditional
Applicant
NuVasive Specialized Orthopedics, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/7/2017
Days to Decision
33 days
Submission Type
Summary

PRECICE Intramedullary Limb Lengthening System

Page Type
Cleared 510(K)
510(k) Number
K170346
510(k) Type
Traditional
Applicant
NuVasive Specialized Orthopedics, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/7/2017
Days to Decision
33 days
Submission Type
Summary