510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K002699Substantially Equivalent

Parietex Composite (Pco) Mesh

Medical Device Consultants, Inc., North Attleboro MA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K002699 is the FDA 510(k) clearance record for PARIETEX COMPOSITE (PCO) MESH, a class II device, cleared for Medical Device Consultants, Inc. on under FDA product code FTL (Mesh, Surgical, Polymeric). FDA records list 14 510(k) clearances for Medical Device Consultants, Inc., from to . As of , FDA records show no recalls naming K002699.

Clearance record

Decision date
Received
(169 days to decision)
Product code
FTL Mesh, Surgical, Polymeric
Regulation
21 CFR 878.3300
Device class
Class II
Review panel
General, Plastic Surgery
Applicant
Medical Device Consultants, Inc. 49 Plain St., North Attleboro MA
510(k) summary
Summary
Third party review
No

Clearances, product code FTL

Trailing 12 months
1 clearance 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 20260
October 20260