510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K101765Substantially Equivalent

Kyphon Anchor Facet Screw System

Medtronic Spine, LLC, Sunnyvale CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K101765 is the FDA 510(k) clearance record for KYPHON ANCHOR FACET SCREW SYSTEM, cleared for Medtronic Spine, LLC on under FDA product code MRW (System, Facet Screw Spinal Device). FDA records list 2 510(k) clearances for Medtronic Spine, LLC, from to . As of , FDA records show no recalls naming K101765.

Clearance record

Decision date
Received
(121 days to decision)
Product code
MRW System, Facet Screw Spinal Device
Device class
Unclassified
Review panel
Unknown
Applicant
Medtronic Spine, LLC 1221 Crossman Ave., Sunnyvale CA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code MRW

Trailing 12 months
7 clearances under product code MRW in the twelve months to October 2026, November 2025 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code MRW, trailing twelve months
MonthClearances
November 20251
December 20251
January 20261
February 20260
March 20261
April 20260
May 20261
June 20261
July 20260
August 20260
September 20261
October 20260