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NBD CEMENT RESTRICTOR DEVICE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K021788
510(k) Type
Traditional
Applicant
New Business Development, LLC
Country
United States
FDA Decision
Substantially Equivalent - With Limitations
Decision Date
10/4/2002
Days to Decision
126 days
Submission Type
Summary

NBD CEMENT RESTRICTOR DEVICE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K021788
510(k) Type
Traditional
Applicant
New Business Development, LLC
Country
United States
FDA Decision
Substantially Equivalent - With Limitations
Decision Date
10/4/2002
Days to Decision
126 days
Submission Type
Summary