510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K213823Substantially Equivalent

Intera Refill Kit

Intera Oncology, Wellesley MA / Special, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K213823 is the FDA 510(k) clearance record for Intera Refill Kit, a class II device, cleared for Intera Oncology, Inc. on under FDA product code PTI (Non-Coring (Huber) Needle). FDA's definition for product code PTI reads: "The non-coring needle (Huber) is utilized to gain access into a subcutaneous implanted intravascular infusion port but can also be used to access other non-vascular implanted devices with similar septums". FDA records list 2 510(k) clearances for Intera Oncology, Inc., from to . As of , FDA records show no recalls naming K213823.

Clearance record

Decision date
Received
(98 days to decision)
Product code
PTI Non-Coring (Huber) Needle
Regulation
21 CFR 880.5570
Device class
Class II
Review panel
General Hospital
Applicant
Intera Oncology, Inc. 65 Williams St., Suite 200, Wellesley MA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code PTI

Trailing 12 months
2 clearances under product code PTI in the twelve months to October 2026, November 2025 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code PTI, trailing twelve months
MonthClearances
November 20251
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20261
October 20260