ACUFEX ENDOBUTTON TAPE— 510(k) K952535
Substantially Equivalent for Some IndicationsAcufex Microsurgical, Inc.
FDA 510(k) clearance K952535 for ACUFEX ENDOBUTTON TAPE, Substantially Equivalent for Some Indications on 1996-02-08. Applicant: Acufex Microsurgical, Inc.. Device class: 2.
Clearance details
- Applicant
- Acufex Microsurgical, Inc.
- Product code
- Code GAT
- Device class
- Class 2
- Regulation
- 21 CFR 878.5000
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent for Some Indications
- Clearance type
- Traditional
- Location
- Mansfield, MA, US
Recent devices under product code GAT
view allMore clearances from Acufex Microsurgical, Inc.
view allAdverse events under product code GAT
product code GAT- Death
- 19
- Injury
- 4,163
- Malfunction
- 8,646
- Other
- 2
- Total
- 12,830
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 →
Recalls naming K952535
K-number listed on FDA's recall record- Z-1536-2018 — Smith & Nephew Whipknot Soft Tissue Cinch #5 Sutures. PN: 7211015
- Z-2745-2016 — Smith & Nephew Whipknot Soft Tissue Cinch (USP#5) suture. PN: 7211015 Used during ligament reconstruction.
Matched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K952535.
Data sourced from openFDA. This site is unofficial and independent of the FDA.