Last synced on 14 November 2025 at 11:06 pm

IMPIX LUMBAR INTERBODY DEVICE

Page Type
Cleared 510(K)
510(k) Number
K100544
510(k) Type
Special
Applicant
MEDICREA TECHNOLOGIES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/22/2010
Days to Decision
147 days
Submission Type
Summary

IMPIX LUMBAR INTERBODY DEVICE

Page Type
Cleared 510(K)
510(k) Number
K100544
510(k) Type
Special
Applicant
MEDICREA TECHNOLOGIES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/22/2010
Days to Decision
147 days
Submission Type
Summary