Last synced on 25 January 2026 at 3:41 am

INTER-OS LIMB LENGTHENER

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K031875
510(k) Type
Traditional
Applicant
Inter-Os Technologies
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/22/2003
Days to Decision
127 days
Submission Type
Summary

INTER-OS LIMB LENGTHENER

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K031875
510(k) Type
Traditional
Applicant
Inter-Os Technologies
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/22/2003
Days to Decision
127 days
Submission Type
Summary