CrossFAST Integrated Microcatheter Advanced Delivery System (K262817): 510(k) cleared for Vantis Vascular, Inc.
CrossFAST Integrated Microcatheter Advanced Delivery System (K262817): 510(k) cleared for Vantis Vascular, Inc. (California): 510(k) cleared for Vantis Vascular, Inc. Its amount of 42 is below the median of 138 (11th percentile). Dated 47 days ago, it serves as a historical benchmark. Score 35/100. As of 2026-11-04, from U.S. FDA openFDA (510(k) clearances and device enforcement reports).
Data as of · Compiled by Zalwin from U.S. FDA openFDA (510(k) clearances and device enforcement reports)
amount: 42 · 11th percentile of 414 FDAPulse records · 0.3x the median
Free preview: all 14 published fields of this record are shown below. Locked: 75 related CA FDAPulse records and the 5-column CSV export.
| Field | Value |
|---|---|
| Record | 510(k) clearance |
| 510(k) number | K262817 |
| Device | CrossFAST Integrated Microcatheter Advanced Delivery System |
| Applicant | Vantis Vascular, Inc. |
| Specialty / panel | Cardiovascular |
| Product code | DQY |
| Device class | 2 |
| Clearance type | Special |
| Decision | Substantially Equivalent |
| Received | 2026-08-07 |
| Decision date | 2026-09-18 |
| Review time (days) | 42 |
| Third-party review | No |
| Applicant location | San Jose, CA, US |
| amount percentile | 11th of 414 (median 138, 0.3x median) |
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CSV columns: Record · Specialty · Date · Review days · Recall class · official source URL
- Source agency: U.S. FDA openFDA (510(k) clearances and device enforcement reports)
- Record date: 2026-09-18
- Data refreshed: 2026-11-04
- Refunds on request within 14 days
Top FDAPulse records (CA first): Triever Duo Catheter (K253419) · Helo Return (K253717) · DistaSense(TM) (v1) (K254058) · BD OneFlow LST; BD OneFlow B-CLPD T1; BD FACSLyric Flow Cyto · CapsoView (CVV); CapsoCloud (CLD) (K254230) · Browse all by state and category →
LIVE PUBLIC DATA Source: U.S. FDA openFDA (510(k) clearances and device enforcement reports) · Last refreshed: Wed, 04 Nov 2026 09:16:12 GMT
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Peer benchmark and outreach value: CrossFAST Integrated Microcatheter Advanced Delivery System (K262817): 510(k) cleared for Vantis Vascular, Inc. and 76 California peers
- California FDAPulse records like this one: 76
- CrossFAST Integrated Microcatheter Advanced Delivery System (K262817): 510(k) cleared for Vantis Vascular, Inc.'s amount: 11th percentile of 414 records
- Timing: Low: older than 30 days
- Estimated pipeline if you contact every California peer: $15,200 (peers × rate × deal size; an estimate from your assumptions, not a forecast)
35 / 100 Predicate Speed & CAPA Advisory Opportunity Score
- Fast 42-day review: this device is a strong predicate for similar products.
- Special 510(k): a modification of an existing device.
What is the FDAPulse record for CrossFAST Integrated Microcatheter Advanced Delivery System (K262817): 510(k) cleared for Vantis Vascular, Inc. in California?
CrossFAST Integrated Microcatheter Advanced Delivery System (K262817) by Vantis Vascular, Inc. was cleared on 2026-09-18 after 42 days of review.
How does CrossFAST Integrated Microcatheter Advanced Delivery System (K262817): 510(k) cleared for Vantis Vascular, Inc. compare to other California FDAPulse records?
Its amount of 42 is below the median (11th percentile); smaller records often move faster and face less competition. It is 47 days old; check the official source for later updates before acting. Its Predicate Speed & CAPA Advisory Opportunity Score of 35/100 is modest; treat it as background rather than a priority.
CrossFAST Integrated Microcatheter Advanced Delivery System (K262817) vs. top 2 peers
| Organization | Location | Record date |
|---|---|---|
| CrossFAST Integrated Microcatheter Advanced Delivery System (K262817) | CA | 2026-09-18 |
| QCA 10 Electrocardiograph (QCARD-10); QCA 10W Electrocardiograph (QCARD-10W) (K260250) | CA | 2026-09-29 |
| DistaSense(TM) (v1) (K254058) | CA | 2026-09-25 |
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