FDA Device Intelligence
HomeHighridge Medical, LLC › Timberline Lateral Fusion System

Timberline Lateral Fusion System

Highridge Medical, LLC · Model 8737-6010 · UDI-DI 03662663275682

FZO
2
510(k) clearances
315
Adverse events
1
Recalls
244
Facilities

Description

BOX CHISEL ANGLED 16MM X 10MM

Recalls

DateFirmReason
2015-06-24Synthes (USA) Products LLCIt was discovered that a 10mm Chisel Blade was etched as a 16mm Chisel Blade.

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.