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PROGENIX® PUTTY and PROGENIX® PLUS

MEDTRONIC SOFAMOR DANEK, INC. · Model 006001 · UDI-DI 00613994391018

NUN Prescription
1
510(k) clearances
121
Adverse events
0
Recalls
23
Facilities

Description

DBM 006001 PROGENIX PLUS 1CC

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.