Last synced on 14 November 2025 at 11:06 pm

MODIFICATION TO ALTIUS OCT SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K043229
510(k) Type
Special
Applicant
INTERPORE CROSS INTL.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/21/2004
Days to Decision
29 days
Submission Type
Summary

MODIFICATION TO ALTIUS OCT SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K043229
510(k) Type
Special
Applicant
INTERPORE CROSS INTL.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/21/2004
Days to Decision
29 days
Submission Type
Summary