MODIFIED RETRIEVER (MODIFIED, LINE EXTENSION), MODELS 90152, 90153— 510(k) K093610
Substantially EquivalentConcentric Medical, Inc.
FDA 510(k) clearance K093610 for MODIFIED RETRIEVER (MODIFIED, LINE EXTENSION), MODELS 90152, 90153, Substantially Equivalent on 2011-02-17. Applicant: Concentric Medical, Inc.. Device class: 2.
Clearance details
- Applicant
- Concentric Medical, Inc.
- Product code
- Product code NRY
- Device class
- Class 2
- Regulation
- 21 CFR 870.1250
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mountain View, CA, US
Recent devices under product code NRY
view all- K262021 — Toro 71 Aspiration Catheter; Toro Aspiration Tubing
- K263266 — Route 92 Medical Full Length 046 Reperfusion System and Aspiration Tubing Set
- K261089 — Radical 064 Reperfusion Catheter; Radical 076 Reperfusion Catheter; Radical Aspiration Tubing Kit
- K260617 — Tigertriever 13 Ultra Revascularization Device
- K262398 — CEREGLIDE 57 Intermediate Catheter; Cerenovus Aspiration Tubing set
More clearances from Concentric Medical, Inc.
view all- K173352 — Trevo Pro Vue Retriever and Trevo XP Pro Vue Retriever (Trevo Retriever)
- DEN150049 — Modified Trevo ProVue Retriever, Trevo XP ProVue Retriever 4x20mm, Trevo XP ProVue Retriever 3x20mm, Trevo XP ProVue Retriever 6x25mm, Trevo XP ProVue Retriever 4x30mm
- K150616 — Trevo XP ProVue Retriever (4x30mm)
- K143077 — Trevo XP ProVue Retriever (6X25mm)
- K133177 — MODIFIED HD GUIDE CATHETER
Adverse events under product code NRY
product code NRY- Death
- 411
- Injury
- 1,712
- Malfunction
- 1,855
- Total
- 3,978
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Data sourced from openFDA. This site is unofficial and independent of the FDA.