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DEPARTMENT OF HEALTH AND HUMAN SERVICES
FOOD AND DRUG ADMINISTRATION
CDRH PREMARKET REVIEW SUBMISSION COVER
Date of Submission
User Fee Payment ID Number
SECTION A
PMA
Form Approval
OMB No. 9010-0120
Expiration Date: May 31, 2007.
SHEET
See OMB Statement on page 5.
FDA Submission Document Number (if known)
TYPE OF SUBMISSION
PMA & HDE Supplement
PDP
510(k)
Meeting
Original Submission:
Pre-510(K) Meeting
Original Submission
Regular (180 day)
Original PDP
Premarket Report
Special
Notice of Completion
Traditional
Pre-IDE Meeting
Modular Submission
Panel Track (PMA Only)
Amendment to PDP
Special
Pre-PMA Meeting
Amendment
30-day Supplement
30-day Notice
Abbreviated (Complete
section I, Page 5)
Pre-PDP Meeting
Report
Report Amendment
135-day Supplement
Licensing Agreement
Real-time Review
Day 100 Meeting
Additional Information
Agreement Meeting
Third Party
Determination Meeting
Other (specify):
Amendment to PMA &
HDE Supplement
Other
IDE
Humanitarian Device
Exemption (HDE)
Class II Exemption Petition
Evaluation of Automatic
Class III Designation
(De Novo)
Original Submission
Original Submission
Original Submission
Original Submission
513(g)
Amendment
Amendment
Additional Information
Supplement
Supplement
Other
(describe submission):
Additional Information
Other Submission
Report
Report Amendment
Have you used or cited Standards in your submission?
SECTION B
Yes
(If Yes, please complete Section I, Page 5)
No
SUBMITTER, APPLICANT OR SPONSOR
Company / Institution Name
Establishment Registration Number (if known)
Division Name (if applicable)
Phone Number (including area code)
Street Address
FAX Number (including area code)
(
(
City
)
)
State / Province
ZIP/Postal Code
Country
Contact Name
Contact Title
SECTION C
Contact E-mail Address
APPLICATION CORRESPONDENT (e.g., consultant, if different from above)
Company / Institution Name
Division Name (if applicable)
Phone Number (including area code)
(
Street Address
(
City
)
FAX Number (including area code)
)
State / Province
ZIP/Postal Code
Country
Contact Name
Contact Title
FORM FDA 3514 (6/05)
Contact E-mail Address
PAGE 1 OF 5 PAGES
PSC Media Arts (301) 443-1090
EF
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SECTION D1
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REASON FOR APPLICATION - PMA, PDP, OR HDE
Withdrawal
Additional or Expanded Indications
Change in design, component, or
specification:
Location change:
Manufacturer
Request for Extension
Software / Hardware
Sterilizer
Post-approval Study Protocol
Color Additive
Packager
Request for Applicant Hold
Material
Request for Removal of Applicant Hold
Specifications
Request to Remove or Add Manufacturing Site
Other (specify below)
Annual or Periodic
Process change:
Manufacturing
Sterilization
Packaging
Other (specify below)
Report Submission:
Post-approval Study
Labeling change:
Indications
Instructions
Adverse Reaction
Device Defect
Amendment
Performance
Shelf Life
Trade Name
Other (specify below)
Response to FDA correspondence:
Change in Ownership
Change in Correspondent
Change of Applicant Address
Other Reason (specify):
SECTION D2
New Device
REASON FOR APPLICATION - IDE
Change in:
Repose to FDA Letter Concerning:
New Indication
Correspondent / Applicant
Conditional Approval
Addition of Institution
Design / Device
Deemed Approved
Expansion / Extension of Study
Informed Consent
Deficient Final Report
IRB Certification
Manufacturer
Deficient Progress Report
Termination of Study
Manufacturing Process
Deficient Investigator Report
Withdrawal of Application
Protocol - Feasibility
Disapproval
Unanticipated Adverse Effect
Protocol - Other
Notification of Emergency Use
Sponsor
Request Extension of
Time to Respond to FDA
Compassionate Use Request
Treatment IDE
Continued Access
Request Meeting
Report submission:
Request Hearing
Current Investigator
Annual Progress Report
Site Waiver Report
Final
Other Reason (specify):
SECTION D3
New Device
REASON FOR SUBMISSION - 510(k)
Additional or Expanded Indications
Change in Technology
Other Reason (specify):
FORM FDA 3514 (6/05)
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SECTION E
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ADDITIONAL INFORMATION ON 510(K) SUBMISSIONS
Summary of, or statement concerning,
safety and effectiveness information
Product codes of devices to which substantial equivalence is claimed
1
2
3
4
5
6
7
8
510 (k) summary attached
510 (k) statement
Information on devices to which substantial equivalence is claimed (if known)
510(k) Number
Manufacturer
Trade or Proprietary or Model Name
1
1
1
2
2
2
3
3
3
4
4
4
5
5
5
6
6
6
SECTION F
PRODUCT INFORMATION - APPLICATION TO ALL APPLICATIONS
Common or usual name or classification
Model Number
Trade or Proprietary or Model Name for This Device
1
1
2
2
3
3
4
4
5
5
FDA document numbers of all prior related submissions (regardless of outcome)
1
2
3
4
5
6
7
8
9
10
11
12
Data Included in Submission
Laboratory Testing
SECTION G
Product Code
Animal Trials
Human Trials
PRODUCT CLASSIFICATION - APPLICATION TO ALL APPLICATIONS
C.F.R. Section (if applicable)
Device Class
Class I
Class II
Class III
Unclassified
Classification Panel
Indications (from labeling)
FORM FDA 3514 (6/05)
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FDA Document Number (if known)
Note: Submission of this information does not affect the need to submit a 2891
or 2891a Device Establishment Registration form.
SECTION H
MANUFACTURING / PACKAGING / STERILIZATION SITES RELATING TO A SUBMISSION
FDA Establishment Registration Number
Original
Add
Delete
Manufacturer
Contract Sterilizer
Contract Manufacturer
Repackager / Relabeler
Company / Institution Name
Establishment Registration Number
Division Name (if applicable)
Phone Number (including area code)
(
Street Address
)
FAX Number (including area code)
(
City
)
State / Province
Contact Title
Contact Name
Delete
Manufacturer
Contract Sterilizer
Contract Manufacturer
Repackager / Relabeler
Company / Institution Name
Establishment Registration Number
Division Name (if applicable)
Phone Number (including area code)
(
)
Street Address
FAX Number (including area code)
City
State / Province
(
Contact Name
Add
)
ZIP/Postal Code
Contact Title
Delete
Manufacturer
Contract Sterilizer
Contract Manufacturer
Repackager / Relabeler
Company / Institution Name
Establishment Registration Number
Division Name (if applicable)
Phone Number (including area code)
(
Street Address
City
FORM FDA 3514 (6/05)
)
FAX Number (including area code)
(
Contact Name
Country
Contact E-mail Address
FDA Establishment Registration Number
Original
Country
Contact E-mail Address
FDA Establishment Registration Number
Original
Add
ZIP/Postal Code
)
State / Province
Contact Title
ZIP/Postal Code
Country
Contact E-mail Address
PAGE 4 OF 5 PAGES
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SECTION I
Reset Form
UTILIZATION OF STANDARDS
Note: Complete this section if your application or submission cites standards or includes a "Declaration of Conformity to a Recognized Standard"
statement.
Standards No.
Standards
Organization
Standards Title
Version
Date
Standards No.
Standards
Organization
Standards Title
Version
Date
Standards No.
Standards
Organization
Standards Title
Version
Date
Standards No.
Standards
Organization
Standards Title
Version
Date
Standards No.
Standards
Organization
Standards Title
Version
Date
Standards No.
Standards
Organization
Standards Title
Version
Date
Standards No.
Standards
Organization
Standards Title
Version
Date
1
2
3
4
5
6
7
Please include any additional standards to be cited on a separate page.
Public reporting burden for this collection of information is estimated to average 0.5 hour per response, including the time for reviewing instructions, searching
existing data sources, gathering and maintaining the data needed, and completing reviewing the collection of information. Send comments regarding this burden
estimate or any other aspect of this collection of information, including suggestions for reducing this burden to:
Food and Drug Administration
CDRH (HFZ-342)
9200 Corporate Blvd.
Rockville, MD 20850
An agency may not conduct or sponsor, and a person is not required to respond to, a collection of information unless it displays a currently valid OMB control
FORM FDA 3514 (6/05)
PAGE 5 OF 5 PAGES
| File Type | application/pdf |
| File Modified | 2007-04-06 |
| File Created | 2003-12-29 |