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PRECICE INTRAMEDULLARY LIMB LENGTHENING SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K131677
510(k) Type
Traditional
Applicant
ELLIPSE TECHNOLOGIES INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/11/2013
Days to Decision
123 days
Submission Type
Summary

PRECICE INTRAMEDULLARY LIMB LENGTHENING SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K131677
510(k) Type
Traditional
Applicant
ELLIPSE TECHNOLOGIES INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/11/2013
Days to Decision
123 days
Submission Type
Summary