510(K) CLEARANCES 51 ▲2RECALLS POSTED 25 ▲2CLASS I 1PMA DECISIONS 50 ▲13WEEK ENDING / FDA DATA AS OF
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K933077Substantially Equivalent for Some Indications

Exeter Intramedullary Bone Plug

Howmedica Corp., Rutherford NJ / Traditional, Substantially Equivalent for Some Indications
FDA source (opens on fda.gov)

K933077 is the FDA 510(k) clearance record for EXETER INTRAMEDULLARY BONE PLUG, a class II device, cleared for Howmedica Corp. on under FDA product code LZN (Cement Obturator). FDA records list 409 510(k) clearances for Howmedica Corp., from to . As of , FDA records show no recalls naming K933077.

Clearance record

Decision date
Received
(692 days to decision)
Product code
LZN Cement Obturator
Regulation
21 CFR 878.3300
Device class
Class II
Review panel
General, Plastic Surgery
Applicant
Howmedica Corp. 359 Veterans Blvd., Rutherford NJ
Third party review
No

Clearances, product code LZN

Trailing 12 months

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

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