STERLING IF SCREW EYELET, MODEL CID3936 AND STERLING CROSS-PIN EYELET, MODEL CID3937— 510(k) K063584

Substantially Equivalent

Regeneration Technologies, Inc.

FDA 510(k) clearance K063584 for STERLING IF SCREW EYELET, MODEL CID3936 AND STERLING CROSS-PIN EYELET, MODEL CID3937, Substantially Equivalent on 2007-05-09. Applicant: Regeneration Technologies, Inc..

Clearance details

Applicant: Regeneration Technologies, Inc.
Product code: Code HWC
Advisory panel: Orthopedic
Date received: 2006-12-01
Decision date: 2007-05-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Alachua, FL, US

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Adverse events under product code HWC

product code HWC

Death: 20
Injury: 15,910
Malfunction: 8,192
Other: 1
Total: 24,123

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.