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ELLIPSE INTRAMEDULLARY LIMB LENGTHENING SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K101997
510(k) Type
Traditional
Applicant
ELLIPSE TECHNOLOGIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/12/2011
Days to Decision
362 days
Submission Type
Summary

ELLIPSE INTRAMEDULLARY LIMB LENGTHENING SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K101997
510(k) Type
Traditional
Applicant
ELLIPSE TECHNOLOGIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/12/2011
Days to Decision
362 days
Submission Type
Summary