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PolyLock Small Bone

FUSION ORTHOPEDICS, LLC · Model SB-TB-1000 · UDI-DI 00840124513730

NDF Prescription
3
510(k) clearances
8
Adverse events
1
Recalls
10
Facilities

Description

TailorsLock Plate

Recalls

DateFirmReason
2013-10-11Zimmer, Inc.Zimmer recently conducted a review of all historic packaging validations at its Zimmer Manufacturing B.V. (ZMBV) facility in Ponce, Puerto Rico. Based on this review, it was determ

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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.