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Recognized a 510(k)/PMA number — showing its clearance record and devices.

Clearance record K203121

Responsive Arthroscopy Thunderbolt System · Responsive Arthroscopy, LLC · decided 2021-04-27 (SESE)

FDA 510(k) database ↗Summary PDF ↗

Devices

BrandModelCompanyProduct codesPrimary DI
Thunderbolt Plate909014-0000RESPONSIVE ORTHOPEDICS LLCJDR MBI00811714035352
Thunderbolt 285958RESPONSIVE ORTHOPEDICS LLCJDR MBI00811714036465
Thunderbolt Suture Assembly909013-0000RESPONSIVE ORTHOPEDICS LLCJDR MBI00811714035345
Thunderbolt 285957RESPONSIVE ORTHOPEDICS LLCJDR MBI00811714036458