H-H NERVE ROOT RETRACTOR— 510(k) K822048

Substantially Equivalent

Holter-Hausner Intl.

FDA 510(k) clearance K822048 for H-H NERVE ROOT RETRACTOR, Substantially Equivalent on 1982-07-22. Applicant: Holter-Hausner Intl.. Device class: 1.

Clearance details

Applicant: Holter-Hausner Intl.
Product code: Code HAO
Device class: Class 1
Regulation: 21 CFR 882.4535
Advisory panel: Neurology
Date received: 1982-07-12
Decision date: 1982-07-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code HAO

K220920 — Matreneu Percutaneous Balloon Compression Kit2022-09-07
K940973 — MULLAN GANGLION MICROCOMPRESSION SET1995-09-29
K951492 — RIB RESECTOR1995-05-18
K943115 — AUTO SUTURE PITUITARY SPINAL RONGEUR1994-07-25
K942967 — AUTO SUTURE SPINAL CURETTE1994-07-20

More clearances from Holter-Hausner Intl.

K875287 — H-H FLUSHING RESERVOIR1988-07-14
K874508 — H-H EXTERNAL VENTRICULAR DRAINAGE COLLECTION BAG1988-01-19
K872284 — H-H HUNTER ACTIVE TENDON IMPLANT PC1987-09-28
K872285 — H-H HUNTER ACTIVE TENDON IMPLANT DC1987-09-28
K872293 — H-H HUNTER ACTIVE TENDON IMPLANT BC1987-09-28

Data sourced from openFDA. This site is unofficial and independent of the FDA.