510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K172032Substantially Equivalent

Modulift Vertebral Body Replacement (VBR) System

Aesculap Implants Systems, LLC, Center Valley PA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K172032 is the FDA 510(k) clearance record for Modulift Vertebral Body Replacement (VBR) System, a class II device, cleared for Aesculap Implants Systems, Inc. on under FDA product code PLR (Spinal Vertebral Body Replacement Device - Cervical). FDA's definition for product code PLR reads: "Vertebral body replacement in the cervical spine". FDA records list 4 510(k) clearances for Aesculap Implants Systems, Inc., from to . As of , FDA records show no recalls naming K172032.

Clearance record

Decision date
Received
(138 days to decision)
Product code
PLR Spinal Vertebral Body Replacement Device - Cervical
Regulation
21 CFR 888.3060
Device class
Class II
Review panel
Orthopedic
Applicant
Aesculap Implants Systems, Inc. 3773 Corporate Pkwy., Center Valley PA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code PLR

Trailing 12 months
2 clearances under product code PLR in the twelve months to October 2026, November 2025 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code PLR, trailing twelve months
MonthClearances
November 20251
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20261
August 20260
September 20260
October 20260