HDC STERILE SELF LIGATING SPIDER SCREW, MODEL SLI,SL2— 510(k) K091390

Substantially Equivalent

Hdc S.R.L.

FDA 510(k) clearance K091390 for HDC STERILE SELF LIGATING SPIDER SCREW, MODEL SLI,SL2, Substantially Equivalent on 2009-07-30. Applicant: Hdc S.R.L..

Clearance details

Applicant: Hdc S.R.L.
Product code: Code OAT
Advisory panel: Dental
Date received: 2009-05-11
Decision date: 2009-07-30
Decision: Substantially Equivalent
Clearance type: Special
Location: Imola, Bologna, IT

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Adverse events under product code OAT

product code OAT

Injury: 355
Total: 355

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.