510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
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K990930Substantially Equivalent

3D Anatomical Mesh

Santerra Medical Technology, Inc., Lake Elmo MN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K990930 is the FDA 510(k) clearance record for 3D ANATOMICAL MESH, a class II device, cleared for Santerra Medical Technology, Inc. on under FDA product code FTL (Mesh, Surgical, Polymeric). FDA records list one 510(k) clearance for Santerra Medical Technology, Inc. As of , FDA records show no recalls naming K990930.

Clearance record

Decision date
Received
(90 days to decision)
Product code
FTL Mesh, Surgical, Polymeric
Regulation
21 CFR 878.3300
Device class
Class II
Review panel
General, Plastic Surgery
Applicant
Santerra Medical Technology, Inc. 5451 Hilltop Ave., Lake Elmo MN
510(k) summary
Summary
Third party review
No

Clearances, product code FTL

Trailing 12 months
2 clearances under product code FTL in the twelve months to October 2026, May 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code FTL, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20261
June 20260
July 20260
August 20260
September 20261
October 20260