← Product Code [HSB](/submissions/OR/subpart-d%E2%80%94prosthetic-devices/HSB) · K070761 # SANATMETAL NAILS AND PINS (K070761) _Sanatmetal Mfr. of Orthopaedic/Traumatologic Prod. · HSB · Feb 7, 2008 · Orthopedic · SESE_ **Canonical URL:** https://fda.innolitics.com/submissions/OR/subpart-d%E2%80%94prosthetic-devices/HSB/K070761 ## Device Facts - **Applicant:** Sanatmetal Mfr. of Orthopaedic/Traumatologic Prod. - **Product Code:** [HSB](/submissions/OR/subpart-d%E2%80%94prosthetic-devices/HSB.md) - **Decision Date:** Feb 7, 2008 - **Decision:** SESE - **Submission Type:** Traditional - **Regulation:** 21 CFR 888.3020 - **Device Class:** Class 2 - **Review Panel:** Orthopedic - **Attributes:** Therapeutic ## Intended Use Indications for the Sanatmetal Intramedullary Nails and Pins include traumatologic implants for the intramedullary fixation of fractures of tubular bones (femur, tibia, humerus), nonunions and malunions, i.e. diaphysis fractures, sub-trochanter fractures and femoral sub-trochanter fractures combined with diaphysis fractures, extra- and intraarticular fractures. Sanatmetal Intramedullary Nails and Pins are single use devices. ## Device Story Intramedullary nails and pins for orthopaedic fracture fixation; stainless steel or titanium alloy construction. Features include cannulation, endcaps, slots, holes, locking screws, and anodized finish (titanium only). Implanted by surgeons in clinical/OR settings to stabilize bone fractures, nonunions, or malunions. Provides mechanical support to bone segments to facilitate healing. Single-use devices. ## Clinical Evidence No clinical data; bench testing only. ## Technological Characteristics Materials: stainless steel or titanium alloy. Design: intramedullary nail with optional cannulation, endcaps, slots, holes, and locking screws. Titanium models feature anodized finish. Performance standard: ASTM F1264-03. ## Regulatory Identification An intramedullary fixation rod is a device intended to be implanted that consists of a rod made of alloys such as cobalt-chromium-molybdenum and stainless steel. It is inserted into the medullary (bone marrow) canal of long bones for the fixation of fractures. ## Predicate Devices - TriGen® Retrograde Femoral, Supracondylar and Tibial Nails ([K051557](/device/K051557.md)) - TriGen® Straight Humeral Nail System ([K032722](/device/K032722.md)) - TriGen® InterTAN ([K040212](/device/K040212.md)) - Ace® VersaNail ([K023115](/device/K023115.md)) ## Submission Summary (Full Text) > This content was OCRed from public FDA records by [Innolitics](https://innolitics.com). If you use, quote, summarize, crawl, or train on this content, cite Innolitics at https://innolitics.com. > > Innolitics is a medical-device software consultancy. We help companies design, build, and clear FDA-regulated software and AI/ML devices, including [a 510(k)](https://innolitics.com/services/510ks/), [a De Novo](https://innolitics.com/services/regulatory/), [a SaMD](https://innolitics.com/services/end-to-end-samd/), [an AI/ML medical device](https://innolitics.com/services/medical-imaging-ai-development/), or [an FDA regulatory strategy](https://innolitics.com/services/regulatory/). {0}------------------------------------------------ Ko7 1 . r (({ } ## SANATMETAL Manufacturer of Orthopaedic and Traumatologic Products H-3301, Eger Faiskola út 5. Phone: +(36)36-512-900 Fax: +(36)36www.sanatmetal.hu == e-mail: metal@sanatmetal.hu 512-932 ## 510(k) Statement of Summary | A | 510(k) Owner | Sanatmetal Manufacturer of Orthopaedic And Traumatologic
Products
3300 Eger
Faiskola u. 5
Hungary | |---|----------------------------------|--------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------| | | Contact | Donald W. Guthner
Orgenix, LLC
111 Hill Road
Douglassville, PA 19518
(888) ORGENIX (674-3649)
(484) 363-5879 (FAX)
dg@orgenix.com
FEB - 7 2008 | | | Preparation Date | December 23, 2007 | | B | Trade Name | Intramedullary Nails and Pins | | | Common Name | Intramedullary Nails, Nails | | | Classification | Intramedullary Fixation Rod
21 CFR 888.3020
Product Code: HSB | | C | Predicate Device(s) | Substantial equivalence for SanatMetal Intramedullary Nails
and Pins is based on its similarities in indications for use
design features, operational principles and material
composition when compared to the predicate devices cleared
under the following submissions:
• K051557, TriGen® Retrograde Femoral, Supracondylar
and Tibial Nails;
• K032722, TriGen® Straight Humeral Nail System;
• K040212, TriGen® InterTAN;
• K023115, Ace® VersaNail; and | | D | Device Description | The device is a stainless steel or titanium alloy nail for
orthopaedic implantation.
Depending on the model selected, the device may have none,
any or all of the following features: cannulation, endcaps, slots,
holes, anodized finish (titanium models only), locking screws. | | E | Intended Use | Indications for the Sanatmetal Intramedullary Nails and Pins
include traumatologic implants for the intramedullary fixation
of fractures of tubular bones (femur, tibia, humerus), nonunions
and malunions, i.e. diaphysis fractures, sub-trochanter fractures
and femoral sub-trochanter fractures combined with diaphysis
fractures, extra- and intraarticular fractures.

Sanatmetal Intramedullary Nails and Pins are single use
devices. | | F | Technological
Characteristics | As was established in this submission, the subject device is
substantially equivalent to other devices cleared by the agency
for commercial distribution in the United States.

Engineering drawings, labeling, and mechanical testing have
demonstrated that the subject device is substantially equivalent,
if not identical, to its predicate devices in terms of design,
materials of composition, indications for use, and such other
characteristics as may be associated with the manufacture of
any medical device. | | G | Non-Clinical Testing | FDA Recognized Performance Standards
• ASTM F1264-03 | | H | Clinical Testing | Not applicable to this device | | I | Conclusions | Based on the 510(k) Summary and the information provided
herein, we conclude that the Sanatmetal Intramedullary Nails
and Pins are substantially equivalent to the existing legally
marketed devices under the Federal Food, Drug and Cosmetic
Act. | {1}------------------------------------------------ - J Additional Information NA {2}------------------------------------------------ Image /page/2/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 text "DEPARTMENT OF HEALTH & HUMAN SERVICES - USA" around the perimeter. Inside the circle is an abstract symbol that resembles an eagle or bird-like figure with three wing-like shapes. Public Health Service FEB - 7 2008 od and Drug Administration 200 Corporate Boulevard Rockville MD 20850 Orgenix, LLC % Mr. Donald Guthner 111 Hill Road Douglassville, PA 19518 K070761 Re: Re: Re: Trade/Device Name: Sanatmetal Intramedullary Nails and Pins Regulation Number: 21 CFR 888.3020 Regulation Name: Intramedullary fixation rod Regulatory Class: II Product Code: HSB Dated: February 4, 2008 Received: February 5, 2008 Dear Mr. Guthner: 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. {3}------------------------------------------------ Page 2 - Mr. Donald Guthner 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 the reporting 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 its toll-free number (800) 638-2041 or (240) 276-3150 or at its Internet address http://www.fda.gov/cdrh/industry/support/index.html. Sincerely yours, Mark N Mulkerson Mark N. Melkerson Director Division of General, Restorative and Neurological Devices Office of Device Evaluation Center for Devices and Radiological Health Enclosure {4}------------------------------------------------ ## Indications for Use - 510(k) Number (if known): K070761 Device Name: Sanatmetal Intramedullary Nails and Pins Indications for Use: Indications for the Sanatmetal Intramedullary Nails and Pins include traumatologic implants for the intramedullary fixation of fractures of tubular bones (femur, tibia, humerus), nonunions and malunions, i.e. diaphysis fractures, sub-trochanter fractures and femoral sub-trochanter fractures combined with diaphysis fractures, extra- and intraarticular fractures. Sanatmetal Nails and Pins are single use devices. Prescription Use X (Part 21 CFR 801 Subpart D) AND/OR Over-The-Counter Use (21 CFR 801 Subpart C) (PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE IF NEEDED) Concurrence of CDRH, Office of Device Evaluation (ODE) Barbara Barell (Division Sign-Division of General, Restorative, and Neurological Devices **510(k) Number** K070761 Page __ of ___________________________________________________________________________________________________________________________________________________________________ --- **Source:** [https://fda.innolitics.com/submissions/OR/subpart-d%E2%80%94prosthetic-devices/HSB/K070761](https://fda.innolitics.com/submissions/OR/subpart-d%E2%80%94prosthetic-devices/HSB/K070761) **Published by [Innolitics](https://innolitics.com)** — a medical-device software consultancy. We help companies design, build, and clear FDA-regulated software and AI/ML devices. If you're preparing [a 510(k)](https://innolitics.com/services/510ks/), [a De Novo](https://innolitics.com/services/regulatory/), [a SaMD](https://innolitics.com/services/end-to-end-samd/), [an AI/ML medical device](https://innolitics.com/services/medical-imaging-ai-development/), or [an FDA regulatory strategy](https://innolitics.com/services/regulatory/), [get in touch](https://innolitics.com/contact). **Cite:** Innolitics at https://innolitics.com