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GAP ENDO-EXO MEDULLARY SYSTEM
Orthopediatrics Canada ULC · Model GAP-LGC200 · UDI-DI 07540194016805
HXZ
Prescription
1
510(k) clearances
513
Adverse events
1
Recalls
246
Facilities
Description
GAP 2.0 LAG THREAD CUTTER
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2020-11-20 | Zimmer Biomet, Inc. | Device has the potential for fracture during use. |
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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsData 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.
