KENNEDY LAD(TM) LIGAMENT AUGMENTATION DEVICE
FDA premarket approval P850069/S011 · decided 1994-11-28
Approval details
- PMA number
- P850069
- Supplement
- S011
- Supplement type
- Normal 180 Day Track
- Supplement reason
- Location Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- KENNEDY LAD(TM) LIGAMENT AUGMENTATION DEVICE
- Generic name
- LIGAMENTS AND TENDONS, SYNTHETIC
- Applicant
- 3M Company
- Date received
- 1994-05-20
- Decision date
- 1994-11-28
- Days to decision
- 192 days
- Decision code
- APPR
- Product code
- LML
- Advisory committee
- Orthopedic
- Expedited review
- No
- Location
- St. Paul, MN
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