GENESYS PRESSFT SUTURE ANCHOR— 510(k) K121890

Substantially Equivalent

Linvatec Corporation D/B/A Conmed Linvatec

FDA 510(k) clearance K121890 for GENESYS PRESSFT SUTURE ANCHOR, Substantially Equivalent on 2012-08-22. Applicant: Linvatec Corporation D/B/A Conmed Linvatec.

Clearance details

Applicant: Linvatec Corporation D/B/A Conmed Linvatec
Product code: Code MAI
Advisory panel: Orthopedic
Date received: 2012-06-28
Decision date: 2012-08-22
Decision: Substantially Equivalent
Clearance type: Special
Location: Largo, FL, 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.