FS 1000 KNEE SYSTEM— 510(k) K991052

Substantially Equivalent

Renaissance Instruments, LLC

FDA 510(k) clearance K991052 for FS 1000 KNEE SYSTEM, Substantially Equivalent on 1999-11-10. Applicant: Renaissance Instruments, LLC.

Clearance details

Applicant: Renaissance Instruments, LLC
Product code: Code JWH
Advisory panel: Orthopedic
Date received: 1999-03-30
Decision date: 1999-11-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Salt Lake City, UT, US

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Adverse events under product code JWH

product code JWH

Death: 26
Injury: 51,564
Malfunction: 9,725
Other: 9
Total: 61,324

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.