510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K093820Substantially Equivalent

Subfix Arthroereisis Implant, Models Sut0065, Sut0080, Sut0090, Sut0100, Sut0115

Memometal Technologies, Bruz, FR / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K093820 is the FDA 510(k) clearance record for SUBFIX ARTHROEREISIS IMPLANT, MODELS SUT0065, SUT0080, SUT0090, SUT0100, SUT0115, a class II device, cleared for Memometal Technologies on under FDA product code HWC (Screw, Fixation, Bone). FDA records list 10 510(k) clearances for Memometal Technologies, from to . As of , FDA records show no recalls naming K093820.

Clearance record

Decision date
Received
(156 days to decision)
Product code
HWC Screw, Fixation, Bone
Regulation
21 CFR 888.3040
Device class
Class II
Review panel
Orthopedic
Applicant
Memometal Technologies Rue Blaise Pascal, Bruz, FR
510(k) summary
Summary PDF
Third party review
No

Clearances, product code HWC

Trailing 12 months
21 clearances under product code HWC in the twelve months to October 2026, May 2026 the highest month at 4.
Show the numbers
Monthly 510(k) clearances under FDA product code HWC, trailing twelve months
MonthClearances
November 20251
December 20251
January 20260
February 20260
March 20262
April 20263
May 20264
June 20262
July 20261
August 20263
September 20264
October 20260