510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K251193Substantially Equivalent

Grafton™ DBM; Grafton Plus™ DBM Paste; Magnifuse™ Bone Graft

Medtronic Sofamor Danek, Memphis TN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K251193 is the FDA 510(k) clearance record for Grafton™ DBM; Grafton Plus™ DBM Paste; Magnifuse™ Bone Graft, a class II device, cleared for Medtronic Sofamor Danek, Inc. on under FDA product code MQV (Filler, Bone Void, Calcium Compound). FDA records list 253 510(k) clearances for Medtronic Sofamor Danek, Inc., from to . As of , FDA records show no recalls naming K251193.

Clearance record

Decision date
Received
(56 days to decision)
Product code
MQV Filler, Bone Void, Calcium Compound
Regulation
21 CFR 888.3045
Device class
Class II
Review panel
Orthopedic
Applicant
Medtronic Sofamor Danek, Inc. 2600 Sofamor Danek Dr., Memphis TN
510(k) summary
Summary PDF
Third party review
No

Clearances, product code MQV

Trailing 12 months
5 clearances under product code MQV in the twelve months to October 2026, February 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code MQV, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20261
March 20260
April 20261
May 20261
June 20261
July 20260
August 20260
September 20261
October 20260