510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
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K180361Substantially Equivalent

MICRORAPTOR REGENESORB Suture Anchor

Smith & Nephew, Inc., Cordova TN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K180361 is the FDA 510(k) clearance record for MICRORAPTOR REGENESORB Suture Anchor, a class II device, cleared for Smith and Nephew, Inc. on under FDA product code MAI (Fastener, Fixation, Biodegradable, Soft Tissue). FDA records list 572 510(k) clearances for Smith and Nephew, Inc., from to . As of , FDA records show no recalls naming K180361.

Clearance record

Decision date
Received
(110 days to decision)
Product code
MAI Fastener, Fixation, Biodegradable, Soft Tissue
Regulation
21 CFR 888.3030
Device class
Class II
Review panel
Orthopedic
Applicant
Smith and Nephew, Inc. 7135 Goodlett Farms Pkwy., Cordova TN
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