AVITENE ULTRA FOAM CAST MICROFIBRILLAR COLLAGEN HEMOSTAT (MCH) SPONGE
FDA premarket approval N17600/S017 · decided 2001-07-11
Approval details
- PMA number
- N17600
- Supplement
- S017
- Supplement type
- Normal 180 Day Track
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- AVITENE ULTRA FOAM CAST MICROFIBRILLAR COLLAGEN HEMOSTAT (MCH) SPONGE
- Generic name
- Agent, absorbable hemostatic, collagen based
- Applicant
- Davol Inc., Sub. C. R. Bard, Inc.
- Date received
- 2000-12-14
- Decision date
- 2001-07-11
- Days to decision
- 209 days
- Decision code
- APPR
- Product code
- LMF
- Advisory committee
- General, Plastic Surgery
- Expedited review
- No
- Location
- Warwick, RI
- Statement
- APPROVAL FOR MODIFICATIONS TO THE SLURRY PREPARATION AND LYOPHILIZATION PROCESS AND ADJUSTMENTS TO THE PRODUCT SPECIFICATIONS RESULTING FROM THESE MANUFACTURING CHANGES.
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510(k) clearances by this applicant
| Record | Firm | Date |
|---|---|---|
| VENTRALIGHT ST MESH (K101851) | Davol Inc., Sub. C. R. Bard, Inc. | 2010-07-15 |
| BARD PERFIX LIGHT PLUG, MODELS 0117050, 0117060, 0117070, 0117080, 0117150, 0117160 (K092032) | Davol Inc., Sub. C. R. Bard, Inc. | 2009-12-08 |
| BARD 3DMAX MESH (K081010) | Davol Inc., Sub. C. R. Bard, Inc. | 2008-10-07 |
| BARD COMPOSITE L/P MESH (K061754) | Davol Inc., Sub. C. R. Bard, Inc. | 2006-10-23 |
| BARD EXTRA LARGE COMPOSIX KUGEL HERNIA PATCH (K061314) | Davol Inc., Sub. C. R. Bard, Inc. | 2006-06-02 |
| SALUTE II DISPOSABLE FIXATION DEVICE, MODELS 0113070, 0113072, 0113073, 0113077, 0113079 (K051848) | Davol Inc., Sub. C. R. Bard, Inc. | 2005-08-11 |
| SALUTE FIXATION SYSTEM (K050610) | Davol Inc., Sub. C. R. Bard, Inc. | 2005-05-25 |
| AQUASENS FLUID MONITORING SYSTEM (K011069) | Davol Inc., Sub. C. R. Bard, Inc. | 2001-08-16 |