510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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Responsive Arthroscopy

Minneapolis, MN, US

RESPONSIVE ARTHROSCOPY appears in FDA device records in Minneapolis, MN. FDA records list 13 510(k) clearances between and , no PMA records and one registered establishment. As of , FDA records show no recalls for this company, and at least one establishment registration is current.

FDA records held for this company

510(k) clearances
13
PMA records
0
Recall records
0
Registered establishments
1

510(k) clearance history

FDA records hold 13 510(k) clearances for Responsive Arthroscopy between 2018 and 2026. The busiest year on record is 2019, with 3. The most recent is 2026, with 1.

Clearances by year, as a table
510(k) clearance decisions for Responsive Arthroscopy, by decision year
YearClearances
20181
20193
20202
20211
20221
20232
20252
20261
510(k) clearances on record, most recent first
K numberDeviceProduct codeDecisionDecision date
K261632Thunderbolt SystemMBISubstantially Equivalent
K253010Mini Superhawk Suture Anchor SystemMBISubstantially Equivalent
K243726Osprey Suture AnchorMBISubstantially Equivalent
K233258Shadow Knotless All-Suture AnchorsMBISubstantially Equivalent
K230094Responsive Arthroscopy Stealth and Mini Stealth All-Suture AnchorsMBISubstantially Equivalent
K222763Responsive Arthroscopy Mustang and Mustang Knotless Suture AnchorsMBISubstantially Equivalent
K203121Responsive Arthroscopy Thunderbolt SystemMBISubstantially Equivalent
K202569Responsive Arthroscopy Interference Screw SystemHWCSubstantially Equivalent
K202153Responsive Arthroscopy Suture Anchor SystemMBISubstantially Equivalent
K190446Responsive Arthroscopy Wedge Push-In Suture AnchorsMBISubstantially Equivalent
K181076Responsive Arthroscopy Wedge Push-In Suture AnchorsMBISubstantially Equivalent
K180951Responsive Arthroscopy Suture Anchor SystemMBISubstantially Equivalent
K180573Responsive Arthroscopy Interference Screw SystemHWCSubstantially Equivalent

Registered establishments

FDA registered establishments for Responsive Arthroscopy, with the product codes listed at each
RegistrationFEIEstablishmentAddressRegistration expiresProduct codes listed
30152007593015200759RESPONSIVE ARTHROSCOPY701 N 3rd Street, Suite 208, Minneapolis, MN 55401 US2026

Registration numbers link to the FDA registration and listing record for that establishment.

FDA product codes

Recall records

No recall records for this company in the ingested FDA data.

Verification record

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Data as of , FDA export datePage updated Source: openFDA, public domain