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Data / Medical devices / United States / Responsive Arthroscopy

Responsive Arthroscopy: FDA-registered device maker in Minneapolis, MN, United States, 11 510(k) clearances

Responsive Arthroscopy is registered with the FDA (registration 3015200759) in Minneapolis, MN, United States. It lists 6 device types. The FDA files 11 510(k) clearances under its listings, the newest dated October 14, 2025. Registered through 2026. FDA data exported November 2, 2026.

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Get makers like this oneWatch Responsive Arthroscopy
FDA registration number
3015200759
Address
701 N 3rd Street, Suite 208, Minneapolis, MN, United States, 55401
Owner or operator
Responsive Arthroscopy (10059367)
Roles
Specification developer
First device listed
December 27, 2018
Registered through
2026
Brand names listed
Agile Instruments, Agile Suture Anchor, Eagle, Eagle and Eagle Knotless Suture Anchors, Falcon, Hornet Suture Anchor, Instruments-Spirit, Hornet, Lightning, Nighthawk, Superhawk, Mini Superhawk, Thunderbolt, Mini Stealth, Stealth, Shadow, Lightning and more

Devices it lists

DeviceProduct codeClassRoleSource
Bit, SurgicalGFG1Specification developeraccessdata.fda.gov
Fastener, Fixation, Nondegradable, Soft TissueMBI2Specification developeraccessdata.fda.gov
Orthopedic Manual Surgical InstrumentLXH1Specification developeraccessdata.fda.gov
Screw, Fixation, BoneHWC2Specification developeraccessdata.fda.gov
Staple, Fixation, BoneJDR2Specification developeraccessdata.fda.gov
Tray, Surgical, InstrumentFSM1Specification developeraccessdata.fda.gov

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided510(k) numberDeviceProduct codeDecisionApplicantSource
October 14, 2025K253010Mini Superhawk Suture Anchor SystemMBISubstantially EquivalentResponsive Arthroscopy, LLCaccessdata.fda.gov
January 30, 2025K243726Osprey Suture AnchorMBISubstantially EquivalentResponsive Arthroscopy, Inc.accessdata.fda.gov
October 23, 2023K233258Shadow Knotless All-Suture AnchorsMBISubstantially EquivalentResponsive Arthroscopy, LLCaccessdata.fda.gov
August 25, 2023K230094Responsive Arthroscopy Stealth and Mini Stealth All-Suture AnchorsMBISubstantially EquivalentResponsive Arthroscopy, LLCaccessdata.fda.gov
October 13, 2022K222763Responsive Arthroscopy Mustang and Mustang Knotless Suture AnchorsMBISubstantially EquivalentResponsive Arthroscopy, LLCaccessdata.fda.gov
April 27, 2021K203121Responsive Arthroscopy Thunderbolt SystemMBISubstantially EquivalentResponsive Arthroscopy, LLCaccessdata.fda.gov
September 23, 2020K202569Responsive Arthroscopy Interference Screw SystemHWCSubstantially EquivalentResponsive Arthroscopy, LLCaccessdata.fda.gov
September 9, 2020K202153Responsive Arthroscopy Suture Anchor SystemMBISubstantially EquivalentResponsive Arthroscopy, LLCaccessdata.fda.gov
March 27, 2019K190446Responsive Arthroscopy Wedge Push-In Suture AnchorsMBISubstantially EquivalentResponsive Arthroscopy, LLCaccessdata.fda.gov
January 3, 2019K180951Responsive Arthroscopy Suture Anchor SystemMBISubstantially EquivalentResponsive Arthroscopy, LLCaccessdata.fda.gov
November 23, 2018K180573Responsive Arthroscopy Interference Screw SystemHWCSubstantially EquivalentResponsive Arthroscopy, LLCaccessdata.fda.gov

Compare with other makers

Updated October 14, 2025. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.