Cleared Traditional

K161568 - Bone Solutions Mixing and Delivery System

K161568 is an FDA 510(k) clearance for Bone Solutions Mixing and Delivery System, manufactured by Bone Solutions, Inc.. The device is a Class 2 General Hospital device with product code FMF cleared through the Traditional 510(k) pathway after a 101-day FDA review.

K161568 · Bone Solutions, Inc. · General Hospital
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Sep 2016
Decision
101d
Days
Class 2
Risk

K161568 is an FDA 510(k) clearance for the Bone Solutions Mixing and Delivery System. Classified as Syringe, Piston (product code FMF), Class II - Special Controls.

Submitted by Bone Solutions, Inc. (Colleyville, US). The FDA issued a Cleared decision on September 16, 2016 after a review of 101 days - within the typical 510(k) review window.

This device falls under the General Hospital FDA review panel, regulated under 21 CFR 880.5860 - the FDA general hospital 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: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the General Hospital review framework, consistent with the majority of Class II 510(k) submissions.

View all Bone Solutions, Inc. devices

FDA 510(k) Submission Details - K161568

510(k) Number K161568 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 07, 2016
Decision Date September 16, 2016
Days to Decision 101 days
Submission Type Traditional
Review Panel General Hospital (HO)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
28d faster than avg
Panel avg: 129d · This submission: 101d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

FMF Device Classification - Class 2, Special Controls

Product Code FMF Syringe, Piston
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 880.5860
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most General Hospital devices follow this clearance model.

Regulatory Peers - FMF Syringe, Piston

All 549
Devices cleared under the same product code (FMF) and FDA review panel - the closest regulatory comparables to K161568.
Disposable Insulin Syringe
K162180 · Berpu Medical Technology Co., Ltd. · Dec 2016
BD 1ml Luer-lok Hypodermic Syringe, BD 1 mL Luer-Lok Hypodermic Syringe with BD Hypodermic Needle or BD Eclipse Hypodermic Needle, BD 1ml Luer-lok Insulin Syringe
K162081 · Becton, Dickinson and Company · Dec 2016
NovoPen Echo
K162602 · Novo Nordisk, Inc. · Oct 2016
Sure-Fine Insulin Syringes
K152879 · Shina Med Corporation · Sep 2016
InPen
K160629 · Companion Medical, Inc. · Jul 2016
SUNGSHIM STERILE SINGLE USE INSULIN SYRINGE
K152803 · Sung Shim Medicare Co., Ltd. · Jul 2016