DevicePMAs@therightstef:P060008_S053 JSON TXT

Approval for: 1) a change of the supplier of toluene; and 2) a change to the incoming toluene specifications. The device is indicated for improving luminal diameter for the treatment of de novo lesions <= 28 mm in length in native coronary arteries >= 2.5 mm to <= 4.00 mm in diameter.

projects that include this document

Unselected / annnotation		Selected / annnotation
blah6_medical_device 0 (0) PMA_Manual 0 (0) PMA_MER 15 (15) test-2 0 (0) blah6 0 (0) med-device 0 (0) consensus_PMA_Age_Indications 0 (0) age_PMA_annotations 0 (0) Age_blah 0 (0) PMA_age_indications 0 (0) updated_tagging_age_PMA_annotations 0 (0)

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DevicePMAs@therightstef:P060008_S053 JSONTXT

projects that include this document

DevicePMAs@therightstef:P060008_S053 JSON TXT