SUPARTZ
FDA premarket approval P980044/S007 · decided 2009-07-07
Approval details
- PMA number
- P980044
- Supplement
- S007
- Supplement type
- 135 Review Track For 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- SUPARTZ
- Generic name
- Acid, hyaluronic, intraarticular
- Applicant
- Seikagaku Corp.
- Date received
- 2008-07-21
- Decision date
- 2009-07-07
- Days to decision
- 351 days
- Decision code
- APPR
- Product code
- MOZ
- Advisory committee
- Orthopedic
- Expedited review
- No
- Location
- Tokyo
- Statement
- APPROVAL FOR THE FOLLOWING CHANGES TO THE MANUFACTURING PROCESS: 1) REPLACEMENT OF WFI MANUFACTURING EQUIPMENT;2) ADDITION OF A SENSOR FOR PREVENTING DOUBLE CAPPING;3) REPLACEMENT OF THE MULTIPLEXER PROCESSOR;4) ADDITION OF A SYRINGE LABEL SENSOR;5) REPLACEMENT OF THE ELECTRONIC BALANCE;6) CHANGE OF KNOCKERS USED TO PUSH RUBBER PISTONS INTO GLASS SYRINGES DURING THE FILLINGMEDIA FILL TEST (MFT);7) ADDITION OF A SECOND FILTRATION TANK IN ORDER TO FACILITATE THE MANUFACTURING OF PLASTIC ANDGLASS S
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510(k) clearances by this applicant
| Record | Firm | Date |
|---|---|---|
| HADGEL, 4 GRAM/SYRINGE (K011544) | Seikagaku Corp. | 2001-08-15 |