FDA.reportPublic FDA data

RESPONSIVE ARTHROSCOPY

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30152007593015200759RESPONSIVE ARTHROSCOPY1N2026-01-01701 N 3rd Street, Suite 208 Minneapolis MN US 55401

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
2258601375125939K253010Mini Superhawk Suture Anchor SystemMBI2025-10-14
2258601588622681K243726Osprey Suture AnchorMBI2025-01-30
2258601339409769K233258Shadow Knotless All-Suture AnchorsMBI2023-10-23
2258601180410789K230094Responsive Arthroscopy Stealth and Mini Stealth All-Suture AnchorsMBI2023-08-25
2258601264993871K222763Responsive Arthroscopy Mustang and Mustang Knotless Suture AnchorsMBI2022-10-13
2258601924221308K203121Responsive Arthroscopy Thunderbolt SystemMBI2021-04-27
2258601226246047K202569Responsive Arthroscopy Interference Screw SystemHWC2020-09-23
2258601614015495K202153Responsive Arthroscopy Suture Anchor SystemMBI2020-09-09
2258601654878311K190446Responsive Arthroscopy Wedge Push-In Suture AnchorsMBI2019-03-27
2258601563015044K180951Responsive Arthroscopy Suture Anchor SystemMBI2019-01-03
2258601765690974K180573Responsive Arthroscopy Interference Screw SystemHWC2018-11-23
2258601215805799
2258601635850442
2258602008405004

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
MBI92025-10-14
HWC22020-09-23