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PRECICE INTRAMEDULLARY LIMB LENGTHENING SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K133289
510(k) Type
Special
Applicant
Ellipse Technologies, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/9/2013
Days to Decision
45 days
Submission Type
Summary

PRECICE INTRAMEDULLARY LIMB LENGTHENING SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K133289
510(k) Type
Special
Applicant
Ellipse Technologies, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/9/2013
Days to Decision
45 days
Submission Type
Summary