Atlas FDA

MODIFIED MEDI-QUET TOURNIQUET, MODEL #2740-00

FDA 510(k) clearance K863551 · decided 1986-10-03

Clearance details

K-number
K863551
Device name
MODIFIED MEDI-QUET TOURNIQUET, MODEL #2740-00
Applicant
Depuy, Inc.
Decision
Substantially Equivalent
Date received
1986-09-12
Decision date
1986-10-03
Days to decision
21 days
Clearance type
Traditional
Advisory committee
Unknown
Location
Warsaw, IN, US
Third-party review
No
Expedited review
No

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Recalls involving this device

No recalls on record reference this clearance.

PMA approvals by this applicant

RecordFirmDate
ATTUNE Revision Knee System (P830055/S360)Depuy, Inc.2026-08-05
LCS® Total Knee System (P830055/S368)Depuy, Inc.2026-07-15
LCS® Total Knee System (P830055/S367)Depuy, Inc.2026-06-29
LCS® Total Knee System (P830055/S366)Depuy, Inc.2026-06-03
LCS® Total Knee System (P830055/S362)Depuy, Inc.2026-04-10
LCS® Total Knee System (P830055/S363)Depuy, Inc.2026-03-27
LCS® Total Knee System (P830055/S361)Depuy, Inc.2026-02-13
LCS® Total Knee System (P830055/S358)Depuy, Inc.2026-02-13