FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

H-H NERVE ROOT RETRACTOR

K Number: K822048 · Decision Jul 22, 1982
Classifications
1
FEI Numbers
211
Registration Numbers
211
Same Product Code
33
Applicant Total
42
Review Days
10

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Basic Information

Device Name
H-H NERVE ROOT RETRACTOR
K Number
K822048
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
882.4535
Medical Specialty
Neurology
Decision
Substantially Equivalent
Applicant
Holter-Hausner Intl.
Date Received
July 12, 1982
Decision Date
July 22, 1982
Product Code
HAO
Advisory Committee
Neurology
Review Advisory Committee
NE
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
HAO Instrument, Surgical, Non-Powered

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Other Clearances by Holter-Hausner Intl.

K Number Device Name
K875287 H-H FLUSHING RESERVOIR
K874508 H-H EXTERNAL VENTRICULAR DRAINAGE COLLECTION BAG
K872285 H-H HUNTER ACTIVE TENDON IMPLANT DC
K872284 H-H HUNTER ACTIVE TENDON IMPLANT PC
K872293 H-H HUNTER ACTIVE TENDON IMPLANT BC
K871351 H-H HARRIS NEONATAL NASAL CANNULA SET FOR CPAP
K870660 H-H EXTERNAL VENTRICULAR DRAIN (EVD) COMP./SYSTEMS
K865075 H-H SUBGALEAL TROCAR
K853436 H-H HUNTER PASSIVE TENDON IMPLANT
K853437 H-H HUNTER TENDON ROD
Search all 42 clearances from Holter-Hausner Intl. →