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ELLIPSE PRECICE INTRAMEDULLARY LIMB LENGTHENING SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K131490
510(k) Type
Traditional
Applicant
ELLIPSE TECHNOLOGIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/23/2014
Days to Decision
245 days
Submission Type
Summary

ELLIPSE PRECICE INTRAMEDULLARY LIMB LENGTHENING SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K131490
510(k) Type
Traditional
Applicant
ELLIPSE TECHNOLOGIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/23/2014
Days to Decision
245 days
Submission Type
Summary