(218 days)
Not Found
No
The summary describes a system of physical bone plates, meshes, and screws made from bioabsorbable materials. There is no mention of software, algorithms, image processing, or any terms related to AI/ML.
No
The device is a bone fixation system used in trauma and reconstructive procedures of the craniofacial skeleton, primarily to maintain alignment of bone fractures. While it assists in healing, its primary function is mechanical fixation rather than direct therapy (e.g., drug delivery, energy delivery for treatment, or direct biological intervention for disease).
No
The device is a bone fixation system used for trauma and reconstructive procedures, specifically to maintain alignment of bone fractures. It is a therapy device, not a diagnostic one.
No
The device description explicitly states it is comprised of "sterile, single-use bone plates, meshes and screws manufactured from composites of hydroxyapatite and poly-L-lactide (HA/PLLA)", which are physical hardware components.
Based on the provided information, this device is not an IVD (In Vitro Diagnostic).
Here's why:
- IVD Definition: In Vitro Diagnostic devices are used to examine specimens taken from the human body (like blood, urine, tissue) to provide information about a person's health.
- Device Description and Intended Use: The OSTEOTRANS™-MX Bioabsorbable Bone Fixation System is a physical implantable device (plates, meshes, and screws) used to fix bones in the craniofacial skeleton during surgical procedures. It is directly applied to the patient's body.
The function of this device is to provide structural support and fixation for bone, not to analyze biological samples for diagnostic purposes.
N/A
Intended Use / Indications for Use
The OSTEOTRANS™-MX Bioabsorbable Bone Fixation System is intended for use in trauma and reconstructive procedures of the craniofacial skeleton, including fracture of the cranium, infant craniofacial surgery (i.e. craniosynostosis, congenital malformations), pediatric reconstructive procedures, reconstructive procedures of the cranium, craniotomy flap fixation.
Product codes
HRS, HWC, GWO, HBW
Device Description
The OSTEOTRANS™-MX Bioabsorbable Bone Fixation System devices are the sterile, single-use bone plates, meshes and screws manufactured from composites of hydroxyapatite and poly-L-lactide (HA/PLLA). Plates, meshes and screws are provided with various shapes and sizes typical of other marketed fixation devices.
Used properly, in the presence of adequate immobilization, the OSTEOTRANS" MX Bioabsorbable Bone Fixation System devices maintain accurate alignment of bone fractures and osteotomies.
Mentions image processing
Not Found
Mentions AI, DNN, or ML
Not Found
Input Imaging Modality
Not Found
Anatomical Site
craniofacial skeleton, cranium
Indicated Patient Age Range
infant, pediatric
Intended User / Care Setting
Not Found
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
Performance data demonstrate that the OSTEOTRANS ""-MX Bioabsorbable Bone Fixation System has the requisite strength and favorable degradation profile to provide sufficient and sustained bone fixation for intended uses.
Key Metrics
Not Found
Predicate Device(s)
K010352, K992355, K971870, K992905, K003549, K062819, K061881
Reference Device(s)
Not Found
Predetermined Change Control Plan (PCCP) - All Relevant Information
Not Found
§ 882.5320 Preformed alterable cranioplasty plate.
(a)
Identification. A preformed alterable cranioplasty plate is a device that is implanted into a patient to repair a skull defect. It is constructed of a material, e.g., tantalum, that can be altered or reshaped at the time of surgery without changing the chemical behavior of the material.(b)
Classification. Class II (performance standards).
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K073006 page 14
510(k) Summary OSTEOTRANS™-MX Bioabsorbable Bone Fixation System
MAY 2 9 2008
Submitter's name : Submitter's address:
Contact Person :
Date prepared:
Trade or proprietary name:
Common or usual name:
Classification name:
Device product code:
Takiron Co., Ltd. 3-13 Azuchi-machi 2-chome, Chuo-ku, Osaka 541-0052, Japan
Kunihiro Hata Regulatory Affairs Specialist 7-1-19, Minatojimaminamimachi, Chuo-ku, Kobe, Hyogo, 650-0047, Japan Phone: +81 78 306 2601 +81 78 306 2606 Fax: October 23, 2007
OSTEOTRANS™-MX Bioabsorbable Bone Fixation System Bioabsorbable bone fixation plate and screw Cranioplasty plate and screw, Bone plate and screw, Class II HRS - 21 CFR 888.3030 Plate, Fixation, Bone HWC - 21 CFR 888.3040 Screw, Fixation, Bone GWO - 21 CFR 882.5320 Plate, Cranioplasty, Preformed, Alterable HBW - 21 CFR 882.5360 Fastener, Plate, Cranioplasty
Establishment Registration Number:
Takiron Co., Ltd. has not yet obtained an Establishment Registration Number.
Legally Marketed Predicate Devices:
-
- Inion Ltd.; Inion CPS 1.5/2.0/2.5 Bioabsorbable Fixation System (K010352)
- Codman & Shurtleff, Inc.; Codman® Craniosorb™ Absorbable Fixation System 3. (K992905, K003549)
-
- Bioplate Inc .; Modified plate design for use in conjunction with the Bioplate Rigid Bone Plating System for Craniomaxillofacial Surgery (K062819)
- Takiron Co., Ltd.; OSTEOTRANSTM-MX Bioabsorbable Bone Fixation System 5. (K061881)
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Intended Use:
The OSTEOTRANS™-MX Bioabsorbable Bone Fixation System is intended for use in trauma and reconstructive procedures of the craniofacial skeleton, including fracture of the cranium, infant craniofacial surgery (i.e. craniosynostosis, congenital malformations), pediatric reconstructive procedures, reconstructive procedures of the cranium, craniotomy flap fixation.
Device Description:
The OSTEOTRANS™-MX Bioabsorbable Bone Fixation System devices are the sterile, single-use bone plates, meshes and screws manufactured from composites of hydroxyapatite and poly-L-lactide (HA/PLLA). Plates, meshes and screws are provided with various shapes and sizes typical of other marketed fixation devices.
Used properly, in the presence of adequate immobilization, the OSTEOTRANS" MX Bioabsorbable Bone Fixation System devices maintain accurate alignment of bone fractures and osteotomies.
Summary of Technology:
The OSTEOTRANS "" - MX Bioabsorbable Bone Fixation System has the same technological characteristics (i.e., design and material) when compared to the predicate devices.
Performance data demonstrate that the OSTEOTRANS ""-MX Bioabsorbable Bone Fixation System has the requisite strength and favorable degradation profile to provide sufficient and sustained bone fixation for intended uses.
Substantial equivalence
The OSTEOTRANS The MX Bioabsorbable Bone Fixation System is indicated for the same uses and anatomical regions as the predicate devices.
The OSTEOTRANS 2011 MX Bioabsorbable Bone Fixation System is identical with the implants in the previously 510(lx) cleared OSTEOTRANS-MX Bioabsorbable Bone Fixation System (K061881) in terms of composition, manufacturing method, sterilization method and packaging solution.
The OSTEOTRANS™-MX Bioabsorbable Bone Fixation System has very similar physical design features and functional characteristics as the other predicate devices. Therefore the OSTEOTRANS MX Bioabsorbable Bone Fixation System is substantially equivalent in design, materials and intended use and principles of operation to the predicate devices.
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DEPARTMENT OF HEALTH & HUMAN SERVICES
Image /page/2/Picture/1 description: The image shows the seal of the Department of Health & Human Services - USA. The seal features a circular arrangement of text around an emblem. The emblem is a stylized depiction of an eagle with its wings spread, clutching a staff or caduceus.
Public Health Service
Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850
MAY 2 9 2008
Takiron Co., Ltd. % Mr. Kunihiro Hata Regulatory Affairs Specialist 7-1-19, Minatojimaminamimachi, Chuo-ku, Kobe, Hyogo, 650-0047 Japan
Re: K073006
Trade/Device Name: OSTEOTRANS™ -MX Bioabsorbable Bone Fixation System Regulation Number: 21 CFR 882.5320 Regulation Name: Preformed alterable cranioplasty plate. Regulatory Class: Class II Product Code: GWO, HBW Dated: April 7, 2008 Received: April 7, 2008
Dear Mr. Hata:
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 use 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 to 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 agencies. 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. Kunihiro Hata
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 Center for Devices and Radiological Health's (CDRH's) Office of Compliance at (240) 276-0120. Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21CFR Part 807.97). For questions regarding postmarket surveillance, please contact CDRH's Office of Surveillance and Biometric's (OSB's) Division of Postmarket Surveillance at (240) 276-3474. For questions regarding of device adverse events (Medical Device Reporting (MDR)), please contact the Division of Surveillance Systems at (240) 276-3464. You may obtain other general information on your responsibilities under the Act from the Division of Small Manufacturers, International and Consumer Assistance at toll-free number (800) 638-2041 or (240) 276-3150 or the Internet address http://www.fda.gov/cdrh/industry/support/index.html.
Sincerely yours,
Mark N Millerson
Mark N. Melkerson 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
Applicant: _ Takiron Co., Ltd. _ 510(k) Number (if known): K073006 Device Name: OSTEOTRANS™-MX Bioabsorbable Bone Fixation System
Indications For Use:
The OSTEOTRANS™-MX Bioabsorbable Bone Fixation System is intended for use in trauma and reconstructive procedures of the craniofacial skeleton, including fracture of the cranium, infant craniofacial surgery (i.e. craniosynostosis, congenital malformations), pediatric reconstructive procedures, reconstructive procedures of the cranium, craniotomy flap fixation.
Prescription Use X (Per 21 CFR 801.109)
OR Over-The-Counter Use
er Use
N/D
(Please do not write below this line-continue on another page if needed) Concurrence of CDRH, Office of Device Evaluation (ODE)
Nuke bul for axa
(Division Sign-Off)
Division of General, Restorative, and Neurological Devices
510(k) Number K073006
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