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KYPHON ANCHOR FACET SCREW SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K101765
510(k) Type
Traditional
Applicant
MEDTRONIC SPINE LLC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/22/2010
Days to Decision
121 days
Submission Type
Summary

KYPHON ANCHOR FACET SCREW SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K101765
510(k) Type
Traditional
Applicant
MEDTRONIC SPINE LLC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/22/2010
Days to Decision
121 days
Submission Type
Summary