510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K923872Substantially Equivalent

Bone Marrow Biopsy System

Straumann USA, LLC, Cambridge MA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K923872 is the FDA 510(k) clearance record for BONE MARROW BIOPSY SYSTEM, a class I device, cleared for The Straumann Co. on under FDA product code GDM (Needle, Aspiration And Injection, Reusable). FDA records list 176 510(k) clearances for Straumann USA, LLC, from to . As of , FDA records show no recalls naming K923872.

Clearance record

Decision date
Received
(134 days to decision)
Product code
GDM Needle, Aspiration And Injection, Reusable
Regulation
21 CFR 878.4800
Device class
Class I
Review panel
General, Plastic Surgery
Applicant
The Straumann Co. One Alewife Center, Cambridge MA
510(k) summary
Summary
Third party review
No

Clearances, product code GDM

Trailing 12 months

FDA records hold no clearances under product code GDM in the trailing twelve months.

FDA records show no clearances under product code GDM in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code GDM, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260