Home › CURVAFIX, INC. › Implant Selection Device
Implant Selection Device
CURVAFIX, INC. · Model ISD-002 · UDI-DI 10855068008607
HTJ
Prescription
4
510(k) clearances
3,468
Adverse events
3
Recalls
372
Facilities
Description
Reusable surgical measurement instrument used when determining the size of the CurvaFix IM Implant to be used in a pelvic fixation procedure.
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2019-05-28 | Zimmer Biomet, Inc. | There is a potential for weak seals of the sterile packaging. |
| 2011-01-27 | Stryker Howmedica Osteonics Corp. | Stryker Orthopaedics has become aware that the 10 mm on the bone remaining depth gage is incorrect thus allowing for the reamer to leave as little as 8.9mm (in a nominal condition) |
| 2009-12-22 | Stryker Howmedica Osteonics Corp. | The Depth Measuring Gauges have 5 scale marking instead of the required 4 scale markings. |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsData 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.