← Product Code [DTD](/submissions/CV/subpart-d%E2%80%94cardiovascular-prosthetic-devices/DTD) · K902889

# A1-A,A1-B,A1-ABP,A1-MBP,A1-Z,A6-A,A6-B,PEH PACE. (K902889)

_Biotronik, GmbH & Co. · DTD · Aug 23, 1990 · Cardiovascular · SESE_

**Canonical URL:** https://fda.innolitics.com/submissions/CV/subpart-d%E2%80%94cardiovascular-prosthetic-devices/DTD/K902889

## Device Facts

- **Applicant:** Biotronik, GmbH & Co.
- **Product Code:** [DTD](/submissions/CV/subpart-d%E2%80%94cardiovascular-prosthetic-devices/DTD.md)
- **Decision Date:** Aug 23, 1990
- **Decision:** SESE
- **Submission Type:** Traditional
- **Regulation:** 21 CFR 870.3620
- **Device Class:** Class 2
- **Review Panel:** Cardiovascular

## Regulatory Identification

A pacemaker lead adaptor is a device used to adapt a pacemaker lead so that it can be connected to a pacemaker pulse generator produced by a different manufacturer.

## Special Controls

*Classification.* Class II (special controls). The special control for this device is the FDA guidance document entitled “Guidance for the Submission of Research and Marketing Applications for Permanent Pacemaker Leads and for Pacemaker Lead Adaptor 510(k) Submissions.”

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**Source:** [https://fda.innolitics.com/submissions/CV/subpart-d%E2%80%94cardiovascular-prosthetic-devices/DTD/K902889](https://fda.innolitics.com/submissions/CV/subpart-d%E2%80%94cardiovascular-prosthetic-devices/DTD/K902889)

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