← Product Code [KNW](/submissions/GU/subpart-b%E2%80%94diagnostic-devices/KNW) · K033616
# TRAPMATIC SYSTEM SET (K033616)
_H.S Hospital Service S.P.A · KNW · Mar 1, 2004 · Gastroenterology, Urology · SESE_
**Canonical URL:** https://fda.innolitics.com/submissions/GU/subpart-b%E2%80%94diagnostic-devices/KNW/K033616
## Device Facts
- **Applicant:** H.S Hospital Service S.P.A
- **Product Code:** [KNW](/submissions/GU/subpart-b%E2%80%94diagnostic-devices/KNW.md)
- **Decision Date:** Mar 1, 2004
- **Decision:** SESE
- **Submission Type:** Traditional
- **Regulation:** 21 CFR 876.1075
- **Device Class:** Class 2
- **Review Panel:** Gastroenterology, Urology
## Indications for Use
This biopsy instrument is used for drawing of osteomedulary substance and or for explantation of bone marrow.
## Device Story
The TrapMatic System® Set is a bone marrow biopsy needle used by clinicians to extract osteomedullary substance and bone marrow samples. The device functions as a manual surgical instrument. It is used in a clinical setting to obtain tissue samples for diagnostic purposes. The output is a physical bone marrow specimen collected within the needle, which the physician then processes for laboratory analysis to aid in clinical decision-making and diagnosis of bone marrow-related conditions.
## Clinical Evidence
No clinical data provided; bench testing only.
## Technological Characteristics
Manual bone marrow biopsy needle. Class II device. Product code KNW. Regulation 21 CFR 876.1075.
## Regulatory Identification
A gastroenterology-urology biopsy instrument is a device used to remove, by cutting or aspiration, a specimen of tissue for microscopic examination. This generic type of device includes the biopsy punch, gastrointestinal mechanical biopsy instrument, suction biopsy instrument, gastro-urology biopsy needle and needle set, and nonelectric biopsy forceps. This section does not apply to biopsy instruments that have specialized uses in other medical specialty areas and that are covered by classification regulations in other parts of the device classification regulations.
## Submission Summary (Full Text)
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510 k | Pag. 32 di 32 |
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| | TRAPMATIC SYSTEM® SET | |
#### MAR - 1 2004 510 (k) SUMMARY
# K033616
| > Applicant | : HS Hospital Service S.p.A.
Via Naro,81 – 00040 Pomezia (Rome) Italy |
|--------------------------|--------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|
| > Contact Person | : H-S Medical, Inc.
Mr. Lucio Improta
1200 Clint Moore Rd. Suite # 1
Boca Raton, FL 33487
Tel. (561)443-3321 - Fax. (561)443-3532
e-mail : hsmedicalinc@aol.com |
| > Submission Date | : November 02, 2003 |
| > Trade Name | : TrapMatic System® Set Bone Marrow Biopsy Needle |
| > Common Name | : Bone Marrow Biopsy Needle |
| > Classification
Name | : 876.1075 - Biopsy instrument |
## な Indication for use:
This biopsy instrument is used for drawing of osteomedulary substance and or for explantation of bone marrow.
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Image /page/1/Picture/1 description: The image shows the logo for the U.S. Department of Health & Human Services. The logo consists of a circular seal with the words "DEPARTMENT OF HEALTH & HUMAN SERVICES - USA" arranged around the perimeter. Inside the circle is an abstract symbol resembling an eagle or bird in flight, composed of three curved lines.
Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850
MAR - 1 2004
HS Hospital Service S.p.A. c/o Mr. Lucio Improta H-S Medical, Inc. 1200 Clint Moore Road, Suite #1 Boca Raton, Florida 33487
Re: K033616
Trade/Device Name: TrapMatic System® Set Regulation Number: 21 CFR 876.1075 Regulation Name: Gastroenterology-urology biopsy instrument Regulatory Class: II Product Code: KNW Dated: November 2, 2003 Received: December 2, 2003
Dear Mr. Improta:
We have reviewed your Section 510(k) premarket notification of intent to market the device referenced above and have determined the device is substantially equivalent (for the indications for usc stated in the enclosure) to legally marketed predicate devices marketed in interstate commerce prior to May 28, 1976, the enactment date of the Medical Device Amendments, or 10 devices that have been reclassified in accordance with the provisions of the Federal Food, Drug, and Cosmetic Act (Act) that do not require approval of a premarket approval application (PMA). You may, therefore, market the device, subject to the general controls provisions of the Act. The general controls provisions of the Act include requirements for annual registration, listing of devices, good manufacturing practice, labeling, and prohibitions against misbranding and adulteration.
If your device is classified (see above) into either class II (Special Controls) or class III (PMA), it may be subject to such additional controls. Existing major regulations affecting your device can be found in the Code of Federal Regulations, Title 21, Parts 800 to 898. In addition, FDA may publish further announcements concerning your device in the Federal Register.
Please be advised that FDA's issuance of a substantial equivalence determination does not mean that FDA has made a determination that your device complies with other requirements of the Act or any Federal statutes and regulations administered by other Federal agencics. You must comply with all the Act's requirements, including, but not limited to: registration and listing (21 CFR Part 807); labeling (21 CFR Part 801); good manufacturing practice requirements as set forth in the quality systems (QS) regulation (21 CFR Part 820); and if applicable, the electronic product radiation control provisions (Sections 531-542 of the Act); 21 CFR 1000-1050.
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### Page 2 - Mr. Lucio Improta
This letter will allow you to begin marketing your device as described in your Section 510(k) premarket notification. The FDA finding of substantial equivalence of your device to a legally marketed predicate device results in a classification for your device and thus, permits your device to proceed to the market.
If you desire specific advice for your device on our labeling regulation (21 CFR Part 801), please contact the Office of Compliance at (301) 594-4659. Also, please note the regulation entitled. "Misbranding by reference to premarket notification" (21CFR Part 807.97). You may obtain other general information on your responsibilities under the Act from the Division of Small Manufacturers, International and Consumer Assistance at its toll-free number (800) 638-2041 or (301) 443-6597 or at its Internet address http://www.fda.gov/cdrh/dsma/dsmamain.html
Sincerely yours,
uriam C. Provost
Celia M. Witten, Ph.D., M.D. Director Division of General, Restorative and Neurological Devices Office of Device Evaluation Center for Devices and Radiological Health
Enclosure
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Indications for Use
510(K): 033616
Device Name : TRAPMATIC® SYSTEM SET
Indications for Use :
This biopsy instrument is used for drawing of Osteomedullary substance and or for explantation of bone marrow.
Prescription Use
(Part 21 CFR 801 Subpart D)
AND/OR
Over-The-Counter Use (21 CFR 807 Subpart C)
# (PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE IF NEEDED)
Concurrence of CDRH, Office of Device Evaluation (ODE)
Miriam C. Provost
(Division Sign-Off) Division of General, Restorative, and Neurological Devices
510(k) Number__Ko 336/k
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**Source:** [https://fda.innolitics.com/submissions/GU/subpart-b%E2%80%94diagnostic-devices/KNW/K033616](https://fda.innolitics.com/submissions/GU/subpart-b%E2%80%94diagnostic-devices/KNW/K033616)
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