510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K101252Substantially Equivalent

Neotract Anchor System Model: Ref 11208

Neotract Inc, Pleasanton CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K101252 is the FDA 510(k) clearance record for NEOTRACT ANCHOR SYSTEM MODEL: REF 11208, a class II device, cleared for Neotract, Inc. on under FDA product code GAT (Suture, Nonabsorbable, Synthetic, Polyethylene). FDA records list 17 510(k) clearances for Neotract, Inc., from to . As of , FDA records show no recalls naming K101252.

Clearance record

Decision date
Received
(72 days to decision)
Product code
GAT Suture, Nonabsorbable, Synthetic, Polyethylene
Regulation
21 CFR 878.5000
Device class
Class II
Review panel
General, Plastic Surgery
Applicant
Neotract, Inc. 4473 Willow Rd., Suite 100, Pleasanton CA
510(k) summary
Statement
Third party review
No

Clearances, product code GAT

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