Aesculap Implant Systems, Inc.

AESCULAP PEEK INTERVERTEBRAL BODY FUSION SYSTEM: A SPACE, CESPACE, PROSPACE, T-SPACE

All identifiers (2)

Aletia (canonical)ALT-001979

FDA 510(k) · US (primary)K071983

Regulatory Registrations

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FDA

ID: K071983

510k

Last Automated Sync

Mar 2026

Last Clinical Review

Not reviewed

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