ALN Optional Vena Cava Filter (FB.010500, FF.010995, FJ.120096, FB.HOOK, FF.HOOK, FJ.HOOK)
FDA 510(k) clearance K241507 · decided 2024-06-26
Clearance details
- K-number
- K241507
- Device name
- ALN Optional Vena Cava Filter (FB.010500, FF.010995, FJ.120096, FB.HOOK, FF.HOOK, FJ.HOOK)
- Applicant
- Aln S.A.R.L.
- Decision
- Substantially Equivalent
- Date received
- 2024-05-28
- Decision date
- 2024-06-26
- Days to decision
- 29 days
- Clearance type
- Special
- Product code
- DTK
- Device class
- 2
- Regulation number
- 870.3375
- Medical specialty
- Cardiovascular
- Advisory committee
- Cardiovascular
- Location
- Bormes Les Mimosas, FR
- Third-party review
- No
- Expedited review
- No
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Similar devices under this product code
Devices cleared under the same product code - the starting set for predicate research.
Recalls involving this device
No recalls on record reference this clearance.