Last synced on 30 May 2025 at 11:05 pm

INTERBODY INNOVATIONS CEMENT RESTRICTOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K051371
510(k) Type
Traditional
Applicant
INTERBODY INNOVATIONS LLP
Country
United States
FDA Decision
Substantially Equivalent - With Limitations
Decision Date
12/6/2005
Days to Decision
194 days
Submission Type
Summary

INTERBODY INNOVATIONS CEMENT RESTRICTOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K051371
510(k) Type
Traditional
Applicant
INTERBODY INNOVATIONS LLP
Country
United States
FDA Decision
Substantially Equivalent - With Limitations
Decision Date
12/6/2005
Days to Decision
194 days
Submission Type
Summary