Bone Rongeurs

FDA 510(k) K852993 · The Huxley Instrument Corp.

Substantially Equivalent

510(k) numberK852993

Submission

Device name
Bone Rongeurs
Applicant
The Huxley Instrument Corp.
Penn Yan, NY, US
Received
July 15, 1985
Decision date
August 7, 1985
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

No product code recorded.

More from The Huxley Instrument Corp.

510(k)DeviceDecision
K852721Bozeman Uterine Forceps, Straight, 10+410 0R 420HCZ · Traditional 09/06/1985SE
K853016Stille Angular Rongeur, 8-3/4 SS 410 · Traditional 08/07/1985SE
K853015Self-Centering Bone Holding Forceps, 10-1/4 SS420GEN · Traditional 07/29/1985SE
K852716Taylor Percussion Hammer SS 410 or 420GWZ · Traditional 07/26/1985SE
K852735Scalpel Handle #7 SS 410 or 420GDZ · Traditional 07/15/1985SE
K852734O.R. Scissors, Straight, 5-1/2+SHP/SHP SS · Traditional 07/15/1985SE
K852732Iris Scissors, Curved, 4-1/2+SS 410 or 420 · Traditional 07/15/1985SE
K852731Lister Bandage Scissors, 5-1/2+SS 410 or 420 · Traditional 07/15/1985SE
K852730Crile Forceps, Striaght, 6-1/4+SS 410 or 420GEN · Traditional 07/15/1985SE
K852729Aalstead Mosq. Forceps, Straight, 5+SS 410 or 420HTD · Traditional 07/15/1985SE

Questions and answers

When was Bone Rongeurs cleared by the FDA?

Bone Rongeurs (K852993) received a 510(k) decision of Substantially Equivalent on August 7, 1985, 23 days after the submission was received.