Last synced on 14 November 2025 at 11:06 pm

RESIDUAL LIMB LENGTHENING SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K141739
510(k) Type
Traditional
Applicant
ELLIPSE TECHNOLOGIES INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/7/2014
Days to Decision
102 days
Submission Type
Summary

RESIDUAL LIMB LENGTHENING SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K141739
510(k) Type
Traditional
Applicant
ELLIPSE TECHNOLOGIES INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/7/2014
Days to Decision
102 days
Submission Type
Summary