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KSF POSTERIOR SPINGAL FIXATOR FOR SEVERE SPONDYLOLISTHESIS

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K950999
510(k) Type
Traditional
Applicant
Buckman Co., Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/25/1996
Days to Decision
328 days
Submission Type
Summary

KSF POSTERIOR SPINGAL FIXATOR FOR SEVERE SPONDYLOLISTHESIS

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K950999
510(k) Type
Traditional
Applicant
Buckman Co., Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/25/1996
Days to Decision
328 days
Submission Type
Summary