510(K) CLEARANCES 51 ▲2RECALLS POSTED 25 ▲2CLASS I 1PMA DECISIONS 50 ▲13WEEK ENDING / FDA DATA AS OF
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K000021Substantially Equivalent

Aesculap Bone Wax

Aesculap Inc, San Diego CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K000021 is the FDA 510(k) clearance record for AESCULAP BONE WAX, cleared for Aesculap, Inc. on under FDA product code MTJ (Wax, Bone). FDA records list 269 510(k) clearances for Aesculap, Inc., from to . As of , FDA records show no recalls naming K000021.

Clearance record

Decision date
Received
(80 days to decision)
Product code
MTJ Wax, Bone
Device class
Unclassified
Review panel
Unknown
Applicant
Aesculap, Inc. 13221 Maricotte Pl., San Diego CA
510(k) summary
Summary
Third party review
No

Clearances, product code MTJ

Trailing 12 months
2 clearances under product code MTJ in the twelve months to November 2026, June 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code MTJ, trailing twelve months
MonthClearances
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20261
July 20260
August 20260
September 20261
October 20260
November 20260