510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K802783Substantially Equivalent

Surgeons Choice Staple, Remove/implant

Hospital Products Intl., Walker MI / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K802783 is the FDA 510(k) clearance record for SURGEONS CHOICE STAPLE, REMOVE/IMPLANT, a class I device, cleared for Hospital Products Intl. on under FDA product code GBN (Catheter, Pediatric, General & Plastic Surgery). FDA records list one 510(k) clearance for Hospital Products Intl. As of , FDA records show no recalls naming K802783.

Clearance record

Decision date
Received
(42 days to decision)
Product code
GBN Catheter, Pediatric, General & Plastic Surgery
Regulation
21 CFR 878.4200
Device class
Class I
Review panel
General, Plastic Surgery
Applicant
Hospital Products Intl. 4221 Richmond Rd., NW, Walker MI
Third party review
No

Clearances, product code GBN

Trailing 12 months

FDA records hold no clearances under product code GBN in the trailing twelve months.

FDA records show no clearances under product code GBN in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code GBN, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260