FDA Device Intelligence
Home › ZIMMER ORTHOPAEDIC SURGICAL PRODUCTS, INC. › NA

NA

ZIMMER ORTHOPAEDIC SURGICAL PRODUCTS, INC. · Model 00-5049-085-00 · UDI-DI 00889024374867

JDY Prescription
8
510(k) clearances
19
Adverse events
1
Recalls
20
Facilities

Recalls

DateFirmReason
2008-06-30Zimmer Inc.The cartridge is brittle and at increased risk of breakage.

Query this across every FDA database — by API.

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

Get your free API keyRead the docs
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.