Bionx Implants, Ltd.
Bionx Implants, Ltd. holds FDA 510(k) medical device clearances, first cleared 1999, most recent 2003.
Top product codes for Bionx Implants, Ltd.
Recent clearances by Bionx Implants, Ltd.
- K030388 — IMPACT SUTURE ANCHOR. MODEL 433510
- K020056 — DUET SUTURE ANCHOR
- K012000 — 1.5MM BONE FIXATION KIT
- K012001 — SMARTSCREW
- K003077 — SMARTSCREW MODEL 222006...227510
- K003757 — THERMOFX MESH
- K000616 — SMARTWEDGE ACL, MODELS 430623, 430628, 430723, 430728, 430823, 430828
- K993074 — SMART NAIL MODELS 521516, 521520,521525, 531516, 531520. 531525
- K993073 — SMART SCREW ACL MODELS 237020, 237025, 237030, 238020, 238025, 238030, 239020, 239025, 239030
- K993453 — MENISCUS ARROW, MODELS 531110, 531113, 531116
- K992947 — CANNULATED SMARTSCREW MODELS 224540C, 224570C
- K992567 — ANATOMICAL BANKART TACK, MODEL 523520A
Data sourced from openFDA. This site is unofficial and independent of the FDA.