510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K133794Substantially Equivalent

4.5Mm Healix Advance Br Anchor, with 2 or 3 Strands of #2 Permacord Suture, 5.5Mm Healix Advance Br Anchor, with 2 or 3

DePuy Mitek, Inc., Raynham MA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K133794 is the FDA 510(k) clearance record for 4.5MM HEALIX ADVANCE BR ANCHOR, WITH 2 OR 3 STRANDS OF #2 PERMACORD SUTURE, 5.5MM HEALIX ADVANCE BR ANCHOR, WITH 2 OR 3, a class II device, cleared for Depuy Mitek, A Johnson & Johnson Company on under FDA product code MAI (Fastener, Fixation, Biodegradable, Soft Tissue). FDA records list 80 510(k) clearances for DePuy Mitek, Inc., from to . As of , FDA records show no recalls naming K133794.

Clearance record

Decision date
Received
(53 days to decision)
Product code
MAI Fastener, Fixation, Biodegradable, Soft Tissue
Regulation
21 CFR 888.3030
Device class
Class II
Review panel
Orthopedic
Applicant
Depuy Mitek, A Johnson & Johnson Company 325 Paramount Dr., Raynham MA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code MAI

Trailing 12 months
5 clearances under product code MAI in the twelve months to October 2026, February 2026 the highest month at 2.
Show the numbers
Monthly 510(k) clearances under FDA product code MAI, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20262
March 20261
April 20260
May 20261
June 20260
July 20260
August 20261
September 20260
October 20260