510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K943986Substantially Equivalent

Link Endo Model Revision Cup

Turnkey Intergration USA, Inc., Indianapolis IN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K943986 is the FDA 510(k) clearance record for LINK ENDO MODEL REVISION CUP, a class II device, cleared for Turnkey Intergration USA, Inc. on under FDA product code HRS (Plate, Fixation, Bone). FDA records list 26 510(k) clearances for Turnkey Intergration USA, Inc., from to . As of , FDA records show no recalls naming K943986.

Clearance record

Decision date
Received
(323 days to decision)
Product code
HRS Plate, Fixation, Bone
Regulation
21 CFR 888.3030
Device class
Class II
Review panel
Orthopedic
Applicant
Turnkey Intergration USA, Inc. 6060 Castleway Dr. W., Indianapolis IN
510(k) summary
Summary
Third party review
No

Clearances, product code HRS

Trailing 12 months
57 clearances under product code HRS in the twelve months to October 2026, March 2026 the highest month at 13.
Show the numbers
Monthly 510(k) clearances under FDA product code HRS, trailing twelve months
MonthClearances
November 20255
December 20255
January 20264
February 20265
March 202613
April 20266
May 20262
June 20265
July 20265
August 20263
September 20264
October 20260