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CENTERPULSE, SPINE-TECH DIVISION CEMENT RESTRICTOR

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K022615
510(k) Type
Special
Applicant
Centerpulse Spine-Tech, Inc.
Country
United States
FDA Decision
Substantially Equivalent - With Limitations
Decision Date
10/29/2002
Days to Decision
83 days
Submission Type
Summary

CENTERPULSE, SPINE-TECH DIVISION CEMENT RESTRICTOR

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K022615
510(k) Type
Special
Applicant
Centerpulse Spine-Tech, Inc.
Country
United States
FDA Decision
Substantially Equivalent - With Limitations
Decision Date
10/29/2002
Days to Decision
83 days
Submission Type
Summary