Cleared Traditional

K895551 - ROCKET BONE MARROW NEEDLE

K895551 is the FDA 510(k) clearance for ROCKET BONE MARROW NEEDLE by A & A Medical, Inc.. It is a Class 1 General & Plastic Surgery device (product code GDM) cleared through the Traditional 510(k) pathway after a 23-day FDA review.

K895551 · A & A Medical, Inc. · General & Plastic Surgery device
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Oct 1989
Decision
23d
Days
Class 1
Risk

K895551 is an FDA 510(k) clearance for the ROCKET BONE MARROW NEEDLE. Classified as Needle, Aspiration And Injection, Reusable (product code GDM), Class I - General Controls.

Submitted by A & A Medical, Inc. (Branford, US). The FDA issued a Cleared decision on October 6, 1989 after a review of 23 days - a notably fast clearance cycle.

This device falls under the General & Plastic Surgery FDA review panel, regulated under 21 CFR 878.4800 - the FDA general and plastic surgery device framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all A & A Medical, Inc. devices

Submission Details

510(k) Number K895551 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 13, 1989
Decision Date October 06, 1989
Days to Decision 23 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
92d faster than avg
Panel avg: 115d · This submission: 23d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code GDM Needle, Aspiration And Injection, Reusable
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 878.4800
What this classification means

Class I devices are subject to general controls only and most are exempt from 510(k) premarket notification. They represent the lowest regulatory burden in the FDA device framework.

Regulatory Peers - GDM Needle, Aspiration And Injection, Reusable

All 15
Devices cleared under the same product code (GDM) and FDA review panel - the closest regulatory comparables to K895551.
ISLAM STERNAL PUNCTURE NEEDLE, CAT #AG-598-OO-E
K903750 · Downs Surgical , Ltd. · Oct 1990
MANAN BONE BIOPSY NEEDLE
K902177 · Manan Medical Products, Inc. · Sep 1990
PLEURA BIOPSY DEVICE
K901995 · Mill-Rose Laboratory · Jul 1990
CORE BIOPSY NEEDLE, CATALOG CODE #54006
K891537 · Dlp, Inc. · Apr 1989
STORZ UNIV IRRIGAT/ASPIRA & PHACOEMULSIFCATION PAC
K882240 · Storz Instrument Co. · Jul 1988
E-Z-EM(R) LUFKIN BIOPSY NEEDLES
K882601 · E-Z-Em, Inc. · Jul 1988