Last synced on 14 November 2025 at 11:06 pm

SATYRNE INTERFLEX MANDIBULAR FIXATION SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K072463
510(k) Type
Traditional
Applicant
SATYRNE MEDICAL
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/29/2007
Days to Decision
90 days
Submission Type
Summary

SATYRNE INTERFLEX MANDIBULAR FIXATION SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K072463
510(k) Type
Traditional
Applicant
SATYRNE MEDICAL
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/29/2007
Days to Decision
90 days
Submission Type
Summary