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The Tether™

ZIMMER BIOMET INC · Model 211H7050 · UDI-DI 00880304865327

QHP Prescription
0
510(k) clearances
275
Adverse events (1 deaths)
0
Recalls
8
Facilities

Description

7.0MM DIA X 50MM VBT ASSY

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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

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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.