Last synced on 14 November 2025 at 11:06 pm

OSTEOMED CRANIAL DISTRACTION SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K121304
510(k) Type
Traditional
Applicant
OSTEOMED
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/22/2012
Days to Decision
113 days
Submission Type
Summary

OSTEOMED CRANIAL DISTRACTION SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K121304
510(k) Type
Traditional
Applicant
OSTEOMED
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/22/2012
Days to Decision
113 days
Submission Type
Summary