PMA Methods- Streamlined PMA
The streamlined PMA is a pilot program in the Division of Clinical Laboratory Devices. A complete PMA is submitted as in a traditional PMA; however, the Streamlined PMA is for a device in which the technology and use are well known to FDA. A Streamlined PMA review may be appropriate for PMAs when there is either:
- an FDA guidance document or other published methods for review which have been evaluated by FDA, or
- an FDA review history dealing with like products (two or more of a kind)
During the protocol and PMA review, the sponsor must be available for an interactive review process. Ideally, prior to beginning studies to determine the safety and effectiveness of the product to be included in this pilot program, the sponsor would submit its protocol for FDA review. Familiarity with the product and protocol as part of this up-front evaluation should streamline the review of the PMA once filed.
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ISO 13485 Internal Auditor Checklist
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Premarket Approval (PMA) agreement with FDA for the medical device companies - the Requirements
Modular PMA agreement with the FDA-Organizing each Module-Manufacturing Module-Class Audit of Manufacturing Facility up to 17 days
Modular PMA agreement with the FDA-Organizing each Module-Manufacturing Module-Class Audit of Manufacturing Facility up to 17 days
U. S. FDA Medical Device Approval Process
U.S. FDA Class I, II, and III products -Similarities / differences with the EU MDD Annex IX Rules-Exempt, 510(k), and PMA device categories-Design Control, Change Control, and DHF files
U.S. FDA Class I, II, and III products -Similarities / differences with the EU MDD Annex IX Rules-Exempt, 510(k), and PMA device categories-Design Control, Change Control, and DHF files
Processes for 510(k) Clearances for In Vitro Diagnostic/IVD Device Products via FDA-CDRH
IVD Validation & Clearance-What procedures are required-How to validate new systems-How to validate existing systems
IVD Validation & Clearance-What procedures are required-How to validate new systems-How to validate existing systems
510(k) Applications Made Simple
510(k) Summary – Executive Summary-Financial Disclosure –Intended Use Statement-SE-Label Requirements
510(k) Summary – Executive Summary-Financial Disclosure –Intended Use Statement-SE-Label Requirements