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Timberline Lateral Fusion System
Highridge Medical, LLC · Model 8734-0030 · UDI-DI 03662663273350
2
510(k) clearances
89
Adverse events
2
Recalls
76
Facilities
Description
LIGHT CABLE LATERAL
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2009-07-01 | Lumitex Inc | Adhesive which is used to attach LightMat to retractor may not have been tested to Medical standards. The vendor provided an adhesive strip that did not conform to Lumitex specifi |
| 2008-10-24 | Biomet Microfixation, Inc. | Fiber optic cable is missing from the Frederick's Converse Retractor Lot # 042408D08. |
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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.