INNOVASIVE DEVICES ROTATOR CUFF FASTENER— 510(k) K951565

Substantially Equivalent

Innovasive Devices, Inc.

FDA 510(k) clearance K951565 for INNOVASIVE DEVICES ROTATOR CUFF FASTENER, Substantially Equivalent on 1995-09-08. Applicant: Innovasive Devices, Inc..

Clearance details

Applicant: Innovasive Devices, Inc.
Product code: Code MBI
Advisory panel: Orthopedic
Date received: 1995-04-04
Decision date: 1995-09-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Hopkinton, MA, US

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Adverse events under product code MBI

product code MBI

Injury: 3,163
Malfunction: 13,006
Other: 2
Total: 16,171

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.