Anchor with Suture
- UID
- IMP/MD/2019/000335_ebf5d2138c2100d19465ca5e1245eb84_d6550d14770cebb4738ad5845a036496
- Device class
- Class D
- Brand name
- Healix Advance Knotless PEEK Anchor
- License holder
- Johnson & Johnson Private Limited
- Approving authority
- CDSCO
- Product information
- The Gryphon PEEK Anchor is indicated for: Shoulder: Rotator Cuff Repair, Bankart Repair, SLAP Lesion Repair, Biceps Tenodesis, Acromio-Clavicular Separation Repair, Deltoid Repair, Capsular Shift or Capsulolabral Reconstruction, Foot/Ankle: Lateral Stabilization, Medial Stabilization, Achilles Tendon Repair; Knee: Medial Collateral Ligament Repair, Lateral Collateral Ligament Repair, Posterior Oblique Ligament Repair, Iliotibial Band Tenodesis, Elbow: Biceps Tendon Reattachment, Ulnar or Radial Collateral Ligament Reconstruction Hip: Capsular Repair, Acetabular Labral Repair
Anchor with Suture is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2019/000335_ebf5d2138c2100d19465ca5e1245eb84_d6550d14770cebb4738ad5845a036496. This device is marketed under the brand name Healix Advance Knotless PEEK Anchor. The license holder is Johnson & Johnson Private Limited, and it is classified as Device Class Class D. The approving authority is CDSCO.
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