(167 days)
No
The description focuses on the mechanical and optical components of the catheter and does not mention any AI/ML capabilities for image analysis, diagnosis, or guidance. The "Mentions AI, DNN, or ML" and "Mentions image processing" sections are explicitly marked as "Not Found".
No
The device is used for observation and delivery of drugs, not for direct therapeutic treatment itself.
Yes
The device description states "This visual examination then allows the physician to diagnose the potential causes of neural distress and pain." which directly indicates its use for diagnosis.
No
The device description clearly outlines physical components like a flexible double lumen catheter, steering handle, and ports, indicating it is a hardware device, not software-only.
No, this device is not an IVD (In Vitro Diagnostic).
Here's why:
- IVD Definition: In Vitro Diagnostics are tests performed on samples taken from the human body, such as blood, urine, or tissue, to detect diseases, conditions, or infections. They are used outside of the body (in vitro) to provide information for diagnosis, monitoring, or screening.
- Device Function: The MYELOTEC VIDEO GUIDED CATHETER is a device used inside the body (in vivo) for direct visualization and delivery of substances within the epidural space of the spine. It is a surgical/interventional device, not a diagnostic test performed on a sample.
- Intended Use: The intended use clearly describes observing anatomy, pathology, and delivering drugs within the body, not analyzing a sample taken from the body.
Therefore, based on the provided information, this device falls under the category of a surgical or interventional device, not an In Vitro Diagnostic.
N/A
Intended Use / Indications for Use
When used with a fiberoptic endoscope, this device can be used in the lumbar and sacral spine for observing epidural anatomy, pathology and delivery of drugs approved for epidural indications.
Product codes
BSO, HRX
Device Description
The MYELOTEC VIDEO GUIDED CATHETER (VGC) consists of a flexible double lumen catheter, steering handle and associated ports for access to the lumens. The catheter has a built in steering mechanism that allows for guiding the soft tip through the epidural space and soft tissues for optimal access to the source of distress. Each lumen is one (1) mm in diameter. The design allows the use of a flexible fiber optic endoscope for visual examination of the area and surrounding tissues at the distal end of the catheter. This visual examination then allows the physician to diagnose the potential causes of neural distress and pain.
The port on the second lumen allows the injection of saline to expand the space and expose the source of distress for viewing and treatment. The port also facilitates the connection of syringes to deliver physician selected therapeutic agents as appropriate to their diagnosis.
Mentions image processing
Not Found
Mentions AI, DNN, or ML
Not Found
Input Imaging Modality
Not Found
Anatomical Site
lumbar and sacral spine
Indicated Patient Age Range
Not Found
Intended User / Care Setting
Hospital/surgery center
Description of the training set, sample size, data source, and annotation protocol
Not Found
Description of the test set, sample size, data source, and annotation protocol
Not Found
Summary of Performance Studies (study type, sample size, AUC, MRMC, standalone performance, key results)
Not Found
Key Metrics (Sensitivity, Specificity, PPV, NPV, etc.)
Not Found
Predicate Device(s)
Reference Device(s)
Not Found
Predetermined Change Control Plan (PCCP) - All Relevant Information
Not Found
§ 888.1100 Arthroscope.
(a)
Identification. An arthroscope is an electrically powered endoscope intended to make visible the interior of a joint. The arthroscope and accessories also is intended to perform surgery within a joint.(b)
Classification. (1) Class II (performance standards).(2) Class I for the following manual arthroscopic instruments: cannulas, currettes, drill guides, forceps, gouges, graspers, knives, obturators, osteotomes, probes, punches, rasps, retractors, rongeurs, suture passers, suture knotpushers, suture punches, switching rods, and trocars. The devices subject to this paragraph (b)(2) are exempt from the premarket notification procedures in subpart E of part 807 of this chapter, subject to the limitations in § 888.9.
0
AUG 1 1 1998
510(k) NOTIFICATION SUMMARY
MYELOTEC, INC. 4000 NORTHFIELD WAY, SUITE 900 ROSWELL, GA 30076
980734/
CONTACT: THOMAS DUNKLE
PHONE: (770) 664-4656 (EXT. 20) FAX: (770) 664-4363
DATE PREPARED: July 13, 1998
DEVICE NAME: PROPRIETARY NAME: CLASS: PANEL: CLASSIFICATION NAME: PRODUCT CODE: REGULATION NUMBER: PREDICATE DEVICE:
CATHETER MYELOTEC VIDEO GUIDED CATHETER II ANESTESIOLOGY CATHETER, CONDUCTION, ANESTHESIA 73BSO 868.5120 RACZ Tun-L-Kath 510(k) number - K954584
DESCRIPTION AND INTENDED USES:
The MYELOTEC VIDEO GUIDED CATHETER (VGC) consists of a flexible double lumen catheter, steering handle and associated ports for access to the lumens. The catheter has a built in steering mechanism that allows for guiding the soft tip through the epidural space and soft tissues for optimal access to the source of distress. Each lumen is one (1) mm in diameter. The design allows the use of a flexible fiber optic endoscope for visual examination of the area and surrounding tissues at the distal end of the catheter. This visual examination then allows the physician to diagnose the potential causes of neural distress and pain.
The port on the second lumen allows the injection of saline to expand the space and expose the source of distress for viewing and treatment. The port also facilitates the connection of syringes to deliver physician selected therapeutic agents as appropriate to their diagnosis.
NEW INDICATIONS FOR USE:
When used with a fiberoptic endoscope, this device can be used in the lumbar and sacral spine for observing epidural anatomy, pathology and delivery of drugs approved for epidural indications.
EQUIVALENCE:
COMPARISON TABLE
| ATTRIBUTE/name: | MYELOTEC VGC | RACZ Tun-L Kath |
|---|---|---|
| WHERE USED | Hospital/surgery center | Hospital/surgery center |
| SUPPLIED STERILE | YES | YES |
| SINGLE USE | YES | YES |
| INSERTION POINT | SACRAL HIATUS | SACRAL HIATUS |
| MODE OF ENTRY | 8 FR. INTRODUCER | 18 GAGE NEEDLE |
| CATHETER LENGTH | ABOUT 12 INCES | ABOUT 33 INCHES |
| LUMEN INNER DIAMETER | 0.039 INCHES | 0.021 INCHES |
| NUMBER OF LUMENS | 2 | 1 |
| ENDOSCOPE CAPABLE | YES | NO |
| STEERABLE | YES | NO |
1
Image /page/1/Picture/1 description: The image shows the seal of the U.S. Department of Health & Human Services. The seal features an abstract design of an eagle with three human profiles incorporated into its body. The text "DEPARTMENT OF HEALTH & HUMAN SERVICES - USA" is arranged in a circular pattern around the eagle.
Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850
AUG | | 1998
Mr. Thomas A. Dunkle Director Quality Assurance/Regulatory Affairs Myelotec, Inc. 4000 Northfield Way, Suite 900 Roswell, Georgia 30076
Re: K980734 Trade Name: Myelotec Video Guided Catheter Regulatory Class: II Product Code: HRX Dated: May 28, 1998 Received: May 29, 1998
Dear Mr. Dunkle:
We have reviewed your Section 510(k) notification of intent to market the device referenced above and we have determined the device is substantially equivalent (for the indications for use stated in the enclosure) to devices marketed in interstate commerce prior to May 28, 1976, the enactment date of the Medical Device Amendments, or to devices that have been reclassified in accordance with the provisions of the Federal Food, Drug, and Cosmetic Act (Act). 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 (Premarket Approval), 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 895. A substantially equivalent determination assumes compliance with the current Good Manufacturing Practice requirement, as set forth in the Quality System Regulation (QS) for Medical Devices: General regulation (21 CFR Part 820) and that, through periodic (QS) inspections, the Food and Drug Administration (FDA) will verify such assumptions. Failure to comply with the GMP regulation may result in regulatory action. In addition, FDA may publish further announcements concerning your device in the Federal Register. Please note: this response to your premarket notification submission does not affect any obligation you might have under sections 531 through 542 of the Act for devices under the Electronic Product Radiation Control provisions, or other Federal laws or regulations.
2
Page 2 - Mr. Thomas A. Dunkle
This letter will allow you to begin marketing your device as described in your 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 and additionally 809.10 for in vitro diagnostic devices), please contact the Office of Compliance at (301) 594-4595. Additionally, for questions on the promotion and advertising of your device, please contact the Office of Compliance at (301) 594-4639.
Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21 CFR 807.97). Other general information on your responsibilities under the Act may be obtained from the Division of Small Manufacturers Assistance at its toll-free number (800) 638-2041 or (301) 443-6597 or at its internet address "http://www.fda.gov/cdrh/dsmamain.html".
Sincerely yours.
Russell H. Morgan
2 Celia M. Witten, Ph.D., M.D. Director Division of General and Restorative Devices Office of Device Evaluation Center for Devices and Radiological Health
Enclosure
3
510(k) NOTIFICATION - MYELOTEC, INC. ROSWELL, GA. 30076
K980734
INTENDED USE/INDICATIONS
INTENDED USE/INDICATIONS - when used with a fiberoptic endoscope, this device can be used for INTENDED ODEXINDICATIONS will and delivery of drugs approved for epidural indications.
Russell S. Lyons for JZD
Prescription Use
(Per 21 CFR 801.109)
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