Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 2 spellings of its name, each linked to the record.
As of Nov 13, 2026, FDA's public records list Responsive Arthroscopy with 13 510(k) clearances. The most recent is a 510(k) clearance dated Jul 20, 2026: Thunderbolt System.
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Date | Record | Source |
|---|---|---|
| Jul 20, 2026 | Thunderbolt SystemK261632 · MBI | 510(k) clearances |
| Oct 14, 2025 | Mini Superhawk Suture Anchor SystemK253010 · MBI | 510(k) clearances |
| Jan 30, 2025 | Osprey Suture AnchorK243726 · MBI | 510(k) clearances |
| Oct 23, 2023 | Shadow Knotless All-Suture AnchorsK233258 · MBI | 510(k) clearances |
| Aug 25, 2023 | Responsive Arthroscopy Stealth and Mini Stealth All-Suture AnchorsK230094 · MBI | 510(k) clearances |
| Oct 13, 2022 | Responsive Arthroscopy Mustang and Mustang Knotless Suture AnchorsK222763 · MBI | 510(k) clearances |
| Apr 27, 2021 | Responsive Arthroscopy Thunderbolt SystemK203121 · MBI | 510(k) clearances |
| Sep 23, 2020 | Responsive Arthroscopy Interference Screw SystemK202569 · HWC | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
