HSA · registration DE0509721Stryker Air™+ All-Inside Meniscal Repair System
- Registration number
- DE0509721
- Model name
- Stryker 2-0 Knot Pusher/Suture Cutter and Slotted Cannula; AIR+™ All-Inside Meniscal Repair System, Curved Up; AIR+™ All-Inside Meniscal Repair System, Curved Down
- Model identifier
- 4721; 4722; 4723
- Registration date
- September 03, 2024
- Risk class
- Class C
- Product owner
- Stryker Endoscopy
- Registrant / registration holder
- STRYKER SINGAPORE PRIVATE LIMITED
The AIR™+ All-Inside Meniscal Repair Device is intended for use as a suture retention device to facilitate percutaneous or endoscopic soft tissue procedures. The AIR™+ All-Inside Meniscal Repair Device is indicated for use in meniscal repairs and allograft transplant procedures. The AIR™+ All-Inside Meniscal Repair Device is intended to be used for anchoring the allograft to the meniscal rim during allograft transplant procedures.
- Product owner address
- 5900 Optical Court, San Jose, CA 95138, United States
- Registrant address
- 38 BEACH ROAD, #23-11, SOUTH BEACH TOWER, Singapore 189767
This page mirrors one row from HSA’s official registered-medical-device workbook. Product owner and registrant are separate published roles; neither is relabeled as the manufacturer. The official NOT_GENERATED value is retained when HSA does not publish a registration number, and the device name remains part of the stable record identity.