ABSORBABLE BONE SCREW— 510(k) K944544

Substantially Equivalent

Johnson & Johnson Professionals, Inc.

FDA 510(k) clearance K944544 for ABSORBABLE BONE SCREW, Substantially Equivalent on 1996-01-26. Applicant: Johnson & Johnson Professionals, Inc..

Clearance details

Applicant: Johnson & Johnson Professionals, Inc.
Product code: Code MAI
Advisory panel: Orthopedic
Date received: 1994-09-15
Decision date: 1996-01-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: East Windsor, NJ, US

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Adverse events under product code MAI

product code MAI

Injury: 1,948
Malfunction: 8,580
Total: 10,528

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.