MITEK GIII ANCHOR— 510(k) K931782

Substantially Equivalent for Some Indications

Mitek Surgical Products, Inc.

FDA 510(k) clearance K931782 for MITEK GIII ANCHOR, Substantially Equivalent for Some Indications on 1994-07-22. Applicant: Mitek Surgical Products, Inc..

Clearance details

Applicant: Mitek Surgical Products, Inc.
Product code: Code JDR
Advisory panel: Orthopedic
Date received: 1993-04-09
Decision date: 1994-07-22
Decision: Substantially Equivalent for Some Indications
Clearance type: Traditional
Location: Norwood, MA, US

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Adverse events under product code JDR

product code JDR

Injury: 726
Malfunction: 663
Other: 1
Total: 1,390

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.