NEUROLOGICAL SPONGES (PATTIES)— 510(k) K791871
Substantially EquivalentCarwild Corp.
FDA 510(k) clearance K791871 for NEUROLOGICAL SPONGES (PATTIES), Substantially Equivalent on 1979-11-05. Applicant: Carwild Corp.. Device class: Unclassified.
Clearance details
- Applicant
- Carwild Corp.
- Product code
- Code EFQ
- Device class
- Unclassified
- Advisory panel
- Unknown
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
Recent devices under product code EFQ
view allMore clearances from Carwild Corp.
view allRecalls naming K791871
K-number listed on FDA's recall record- Z-2639-2026 — Brand Name: Pilling Wecksorb Product Name: Pilling Wecksorb Neurosponges (Cotton) Pilling¿ Wecksorb Neurosponge Strips (Cotton) Model/Catalog Number: 200100 200101 200102 200103 200104 200105 200106 200108 200110 200112 200120 200121 200123 200131 Software Version: N/A Product Description: Wecksorb Neurosponges are made of an absorbent cotton material. Certain Neurosponge varieties are available with an x-ray detectable thread to assist with location within the surgical site. Some Neurosponges (patties) have a string for accountability during the post-surgical verification process. Wecksorb Neurosponges are for use in the protection of tissue during surgical procedures; tissues include the brain and other central nervous system tissues. Neuro sponges are used during cranial and spine surgery to moisten the dura or to cushion against bone edges. They are also used to protect brain tissue under the dura or elsewhere during incision. Component: N/A
- Z-0772-2023 — Pilling Wecksorb Cylindrical Sponges
Matched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K791871.
Data sourced from openFDA. This site is unofficial and independent of the FDA.