Date de décision2020-07-31
Code produitNLM
Comité consultatifPolitique : medical-regulatory-v1.
GUIDELINES FOR MEDICAL DEVICE REGULATION
1. Introduction
1.1 This document outlines the regulatory requirements for medical devices as established by the U.S. Food and Drug Administration (FDA).
1.2 These guidelines are intended to assist companies in understanding and complying with the applicable regulations for the marketing and sale of medical devices in the United States.
2. Classification of Medical Devices
2.1 Medical devices are classified into three classes (I, II, and III) based on the risk they pose to the user.
2.2 Class I devices are considered lowest risk and typically require a 510(k) submission to the FDA.
2.3 Class II devices are considered moderate risk and may require a Pre-Market Approval (PMA) or a 510(k) submission.
2.4 Class III devices are considered highest risk and generally require a PMA submission.
3. 510(k) Submission
3.1 A 510(k) submission is a pre-market notification submitted to the FDA to demonstrate that a new medical device is substantially equivalent to an existing device that is legally marketed in the United States.
3.2 The 510(k) submission must include a detailed description of the device, its intended use, and the data to support its safety and effectiveness.
4. Pre-Market Approval (PMA)
4.1 A Pre-Market Approval (PMA) is a submission required for certain high-risk medical devices.
4.2 The PMA submission must include extensive clinical data, including the results of clinical trials, to demonstrate the safety and effectiveness of the device.
5. Investigational Device Exemptions (IDE)
5.1 An Investigational Device Exemption (IDE) is a regulatory pathway that allows for the investigation of a new medical device in clinical studies.
5.2 An IDE submission must include a detailed description of the device, the study protocol, and the rationale for the investigation.
6. Good Manufacturing Practices (GMP)
6.1 Good Manufacturing Practices (GMP) are regulations that ensure the quality of medical devices.
6.2 Companies must comply with GMP requirements to ensure that their devices are safe and effective.
7. Labeling and Advertising
7.1 Labeling and advertising of medical devices must comply with FDA regulations.
7.2 Companies must ensure that their labeling and advertising are accurate, clear, and not misleading.
8. Post-Market Surveillance
8.1 Post-market surveillance is a process used to monitor the safety and effectiveness of medical devices after they have been marketed.
8.2 Companies are required to report any adverse events or changes in the device's performance to the FDA.
9. Conclusion
9.1 These guidelines provide a comprehensive overview of the regulatory requirements for medical devices in the United States.
9.2 Companies are encouraged to consult with the FDA or a regulatory expert to ensure compliance with all applicable regulations.
DécisionÉquivalence substantielle
Résumé du dispositif
Reprocessed Endoscopic Trocars and Sleeves is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Sustainability Solutions. It received FDA 510(k) clearance on 2020-07-31 under 510(k) number K201511. The device is classified under product code NLM. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.
Questions fréquentes
What is the Reprocessed Endoscopic Trocars and Sleeves?
Reprocessed Endoscopic Trocars and Sleeves is a medical device that received FDA 510(k) clearance on 2020-07-31. The listed applicant is Stryker Sustainability Solutions. The 510(k) number is K201511.
When did Reprocessed Endoscopic Trocars and Sleeves receive FDA 510(k) clearance?
Reprocessed Endoscopic Trocars and Sleeves received FDA 510(k) clearance on 2020-07-31, under 510(k) number K201511.
Who is the listed applicant for Reprocessed Endoscopic Trocars and Sleeves?
The FDA 510(k) record lists Stryker Sustainability Solutions as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Reprocessed Endoscopic Trocars and Sleeves?
The FDA product code for Reprocessed Endoscopic Trocars and Sleeves is NLM.
Essais cliniques associés
Les enregistrements connexes sont mis en correspondance automatiquement à l'aide des noms, codes produits ou autres métadonnées. Une mise en correspondance n'établit pas de relation clinique, scientifique, corporative ou réglementaire vérifiée ; veuillez consulter les sources officielles liées.
Autres dossiers indiquant Stryker Sustainability Solutions en tant que demandeur
Les enregistrements connexes sont mis en correspondance automatiquement à l'aide des noms, codes produits ou autres métadonnées. Une mise en correspondance n'établit pas de relation clinique, scientifique, corporative ou réglementaire vérifiée ; veuillez consulter les sources officielles liées.
K260636Rémanufacturé LigaSure XP Maryland Ciseau/Diviseur Sans Nano-coatingK250898Reprocessés CISEAU HARMONIC 700 (HAR723/Reprocessés CISEAU HARMONIC 700, ciseaux de diamètre 5mm avec hémostase avancée x 23cm); Reprocessés CISEAU HARMONIC 700 (HAR736/Reprocessés CISEAU HARMONIC 700, ciseaux de diamètre 5mm avec hémostase avancée x 36cm); Reprocessés CISEAU HARMONIC 700 (HAR745/Reprocessés CISEAU HARMONIC 700, ciseaux de diamètre 5mm avec hémostase avancée x 45cm)K241758Réévalué RD SET Capteur d'oxymétrie de pouls Adt (4000); Réévalué RD SET Capteur d'oxymétrie de pouls Pdt (4001); Réévalué RD SET Capteur d'oxymétrie de pouls Inf (4002); Réévalué RD SET Capteur d'oxymétrie de pouls Adt (4003)K241606Ciseaux HARMONIC 1100 réconditionnés, diamètre de 5 mm, longueur de 20 cm (HAR1120) ; Ciseaux HARMONIC 1100 réconditionnés, diamètre de 5 mm, longueur de 36 cm (HAR1136)K233471Écouteurs HARMONIC 1100, diamètre 5 mm, longueur 20 cm (HAR1120) ; Écouteurs HARMONIC 1100, diamètre 5 mm, longueur 36 cm (HAR1136)K231621Cathéter ICE ViewFlex Xtra réconditionné (D087031) Voir tous les 25 dispositifs →
Dispositifs connexes (Code : NLM)
Les enregistrements connexes sont mis en correspondance automatiquement à l'aide des noms, codes produits ou autres métadonnées. Une mise en correspondance n'établit pas de relation clinique, scientifique, corporative ou réglementaire vérifiée ; veuillez consulter les sources officielles liées.
Source officielle
Voir dans la base de données FDA →Données issues de l'API ouverte de la FDA. Pour les informations les plus récentes et faisant autorité, veuillez toujours vous référer au registre officiel.