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KSF POSTERIOR SPINGAL FIXATOR FOR SEVERE SPONDYLOLISTHESIS

Page Type
Cleared 510(K)
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)
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