510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K822109Substantially Equivalent

Shovel Retractor

Bio-Blitz, Inc., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K822109 is the FDA 510(k) clearance record for SHOVEL RETRACTOR, a class I device, cleared for Bio-Blitz, Inc. on under FDA product code NBH (Accessories, Arthroscopic). FDA records list 2 510(k) clearances for Bio-Blitz, Inc., from to . As of , FDA records show no recalls naming K822109.

Clearance record

Decision date
Received
(11 days to decision)
Product code
NBH Accessories, Arthroscopic
Regulation
21 CFR 888.1100
Device class
Class I
Review panel
Orthopedic
Applicant
Bio-Blitz, Inc. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code NBH

Trailing 12 months

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

FDA records show no clearances under product code NBH in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code NBH, 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