Age, weight and ethnicity: information unknown/not provided.(b)(6).The intraocular lens (iol) is not available for evaluation; therefore, a failure analysis of the complaint device cannot be completed.A review of the device history record, complaint trending, and risk documentation for this device will be performed.Upon completion of the review, if there is any further relevant information a supplemental medwatch will be filed.All pertinent information available to johnson & johnson surgical vision, inc.Has been submitted.
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Patient information that was missed in initial mdr, is captured in this supplemental report.Following fields are updated as the result: section a2: date of birth: (b)(6); section a3: gender: male.All pertinent information available to johnson & johnson surgical vision, inc.Has been submitted.
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