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Countersink

CURVAFIX, INC. · Model CCB-002 · UDI-DI 10855068008485

HWW Prescription
0
510(k) clearances
15
Adverse events
17
Recalls
112
Facilities

Description

A T-handled instrument used to manually enlarge the diameter of the proximal portion of bone canal in preparation for insertion of the CurvaFix Implant.

Recalls

DateFirmReason
2019-04-08Zimmer GmbHAn investigation identified that the products were possibly manufactured from a different material than defined in the applicable specifications.
2019-04-08Zimmer GmbHAn investigation identified that the products were possibly manufactured from a different material than defined in the applicable specifications.
2019-04-08Zimmer GmbHAn investigation identified that the products were possibly manufactured from a different material than defined in the applicable specifications.
2019-04-08Zimmer GmbHAn investigation identified that the products were possibly manufactured from a different material than defined in the applicable specifications.
2019-04-08Zimmer GmbHAn investigation identified that the products were possibly manufactured from a different material than defined in the applicable specifications.
2019-04-08Zimmer GmbHAn investigation identified that the products were possibly manufactured from a different material than defined in the applicable specifications.
2019-04-08Zimmer GmbHAn investigation identified that the products were possibly manufactured from a different material than defined in the applicable specifications.
2019-04-08Zimmer GmbHAn investigation identified that the products were possibly manufactured from a different material than defined in the applicable specifications.
2019-04-08Zimmer GmbHAn investigation identified that the products were possibly manufactured from a different material than defined in the applicable specifications.
2019-04-08Zimmer GmbHAn investigation identified that the products were possibly manufactured from a different material than defined in the applicable specifications.

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.