FDA Device Intelligence
Home › BK MEDITECH CO.,LTD. › PIN SCREW

PIN SCREW

BK MEDITECH CO.,LTD. · Model 31730-30-07 · UDI-DI 08809155854078

JDW Prescription
1
510(k) clearances
2,172
Adverse events (2 deaths)
100
Recalls
178
Facilities

Description

Cortical Pin Screw, 3mm Shaft Diameter x 3mm Thread Diameter x 70mm Total Length x 30mm Thread Length

Recalls

DateFirmReason
2018-09-27Orthofix SrlAs a result of complaint investigations it was determined that batches of drill bits have a geometrical detail that does not correspond to the intended design. This could result i
2018-09-27Orthofix SrlAs a result of complaint investigations it was determined that batches of drill bits have a geometrical detail that does not correspond to the intended design. This could result i
2018-09-27Orthofix SrlAs a result of complaint investigations it was determined that batches of drill bits have a geometrical detail that does not correspond to the intended design. This could result i
2018-09-27Orthofix SrlAs a result of complaint investigations it was determined that batches of drill bits have a geometrical detail that does not correspond to the intended design. This could result i
2018-09-27Orthofix SrlAs a result of complaint investigations it was determined that batches of drill bits have a geometrical detail that does not correspond to the intended design. This could result i
2018-09-27Orthofix SrlAs a result of complaint investigations it was determined that batches of drill bits have a geometrical detail that does not correspond to the intended design. This could result i
2018-09-27Orthofix SrlAs a result of complaint investigations it was determined that batches of drill bits have a geometrical detail that does not correspond to the intended design. This could result i
2018-09-27Orthofix SrlAs a result of complaint investigations it was determined that batches of drill bits have a geometrical detail that does not correspond to the intended design. This could result i
2018-09-27Orthofix SrlAs a result of complaint investigations it was determined that batches of drill bits have a geometrical detail that does not correspond to the intended design. This could result i
2018-09-27Orthofix SrlAs a result of complaint investigations it was determined that batches of drill bits have a geometrical detail that does not correspond to the intended design. This could result i

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 docs
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.