Last synced on 19 July 2024 at 11:05 pm

INTER-OS BONE GENERATOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K993869
510(k) Type
Traditional
Applicant
INTER-OS TECHNOLOGIES, L.L.C.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/19/2000
Days to Decision
65 days
Submission Type
Summary

INTER-OS BONE GENERATOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K993869
510(k) Type
Traditional
Applicant
INTER-OS TECHNOLOGIES, L.L.C.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/19/2000
Days to Decision
65 days
Submission Type
Summary